Canonical Allele Identifier: CA1300258785
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870581G= , CM000664.2:g.155870581G= GRCh38
NC_000002.11:g.156727093G= , CM000664.1:g.156727093G= GRCh37
NC_000002.10:g.156435339G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3394C=
XR_001739749.1:n.331-29597C=
XR_001739750.1:n.331-29597C=
XR_001739751.1:n.331-29597C=
XR_923501.2:n.331-3394C=