Canonical Allele Identifier: CA1283591732
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120551854C= , CM000664.2:g.120551854C= GRCh38
NC_000002.11:g.121309430C= , CM000664.1:g.121309430C= GRCh37
NC_000002.10:g.121025900C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923262.1:n.1487+34G=
XR_001739680.2:n.1495+34G=
XR_001739681.2:n.2128+34G=
XR_001739682.1:n.1495+34G=
XR_002959417.1:n.1495+34G=