Canonical Allele Identifier: CA1697889748
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897579C= , CM000669.2:g.30897579C= GRCh38
NC_000007.13:g.30937194C= , CM000669.1:g.30937194C= GRCh37
NC_000007.12:g.30903719C= NCBI36
NG_007475.2:g.49186C=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14414C=