Canonical Allele Identifier: CA1697889672
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897417A= , CM000669.2:g.30897417A= GRCh38
NC_000007.13:g.30937032A= , CM000669.1:g.30937032A= GRCh37
NC_000007.12:g.30903557A= NCBI36
NG_007475.2:g.49024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509504.2:c.621+14424A=