Canonical Allele Identifier: CA1439212736
Gene:

Linked Data

dbSNP Id: rs1711582089

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578114G>C , CM000666.2:g.12578114G>C GRCh38
NC_000004.11:g.12579738G>C , CM000666.1:g.12579738G>C GRCh37
NC_000004.10:g.12188836G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31228C>G
XR_001741374.1:n.254+44541C>G
XR_925406.3:n.140+31228C>G