Canonical Allele Identifier: CA1322177761
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934702A= , CM000664.2:g.203934702A= GRCh38
NC_000002.11:g.204799425A= , CM000664.1:g.204799425A= GRCh37
NC_000002.10:g.204507670A= NCBI36
NG_011586.1:g.2923A= , LRG_65:g.2923A=

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1406T=
XR_001739861.1:n.1566T=
XR_427213.3:n.474+1406T=