Canonical Allele Identifier: CA537204539
Gene:

Linked Data

dbSNP Id: rs1185992604

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870664G>T , CM000664.2:g.155870664G>T GRCh38
NC_000002.11:g.156727176G>T , CM000664.1:g.156727176G>T GRCh37
NC_000002.10:g.156435422G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3477C>A
XR_001739749.1:n.331-29680C>A
XR_001739750.1:n.331-29680C>A
XR_001739751.1:n.331-29680C>A
XR_923501.2:n.331-3477C>A