rs143075508

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Species

Homo sapiens

Symbol

rs143075508

Category

Variant

Variant type

SNP

Overlaps

ABCA12

Location

2:214931790

Nucleotide Change

G>A

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000002.12:g.214931790G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000272895.12:c.*844C>T
• ENSEMBL:ENST00000607412.2:n.351-16035G>A

Show All 18

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences