Canonical Allele Identifier: CA1038177569
Gene:

Linked Data

dbSNP Id: rs1233274219

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870607A>T , CM000664.2:g.155870607A>T GRCh38
NC_000002.11:g.156727119A>T , CM000664.1:g.156727119A>T GRCh37
NC_000002.10:g.156435365A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3420T>A
XR_001739749.1:n.331-29623T>A
XR_001739750.1:n.331-29623T>A
XR_001739751.1:n.331-29623T>A
XR_923501.2:n.331-3420T>A