Canonical Allele Identifier: CA1697889753
Gene:

Linked Data

dbSNP Id: rs576162886

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897584A>C , CM000669.2:g.30897584A>C GRCh38
NC_000007.13:g.30937199A>C , CM000669.1:g.30937199A>C GRCh37
NC_000007.12:g.30903724A>C NCBI36
NG_007475.2:g.49191A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14409A>C