Canonical Allele Identifier: CA1261549153
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711980A= , CM000664.2:g.74711980A= GRCh38
NC_000002.11:g.74939107A= , CM000664.1:g.74939107A= GRCh37
NC_000002.10:g.74792615A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.293A=