Canonical Allele Identifier: CA1038177572
Gene:

Linked Data

dbSNP Id: rs1683149132

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870620A>G , CM000664.2:g.155870620A>G GRCh38
NC_000002.11:g.156727132A>G , CM000664.1:g.156727132A>G GRCh37
NC_000002.10:g.156435378A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3433T>C
XR_001739749.1:n.331-29636T>C
XR_001739750.1:n.331-29636T>C
XR_001739751.1:n.331-29636T>C
XR_923501.2:n.331-3433T>C