Canonical Allele Identifier: CA1300258878
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870780A= , CM000664.2:g.155870780A= GRCh38
NC_000002.11:g.156727292A= , CM000664.1:g.156727292A= GRCh37
NC_000002.10:g.156435538A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3593T=
XR_001739749.1:n.331-29796T=
XR_001739750.1:n.331-29796T=
XR_001739751.1:n.331-29796T=
XR_923501.2:n.331-3593T=