Canonical Allele Identifier: CA759294286
Gene:

Linked Data

dbSNP Id: rs1452603657

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870342A>C , CM000664.2:g.155870342A>C GRCh38
NC_000002.11:g.156726854A>C , CM000664.1:g.156726854A>C GRCh37
NC_000002.10:g.156435100A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3155T>G
XR_001739749.1:n.331-29358T>G
XR_001739750.1:n.331-29358T>G
XR_001739751.1:n.331-29358T>G
XR_923501.2:n.331-3155T>G