Canonical Allele Identifier: CA1697889754
Gene:

Linked Data

dbSNP Id: rs74326065

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897585C>A , CM000669.2:g.30897585C>A GRCh38
NC_000007.13:g.30937200C>A , CM000669.1:g.30937200C>A GRCh37
NC_000007.12:g.30903725C>A NCBI36
NG_007475.2:g.49192C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14408C>A