Canonical Allele Identifier: CA1697889728
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897538A= , CM000669.2:g.30897538A= GRCh38
NC_000007.13:g.30937153A= , CM000669.1:g.30937153A= GRCh37
NC_000007.12:g.30903678A= NCBI36
NG_007475.2:g.49145A=

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14455A=