Canonical Allele Identifier: CA93117926
Gene:

Linked Data

dbSNP Id: rs775176343

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578296G>C , CM000666.2:g.12578296G>C GRCh38
NC_000004.11:g.12579920G>C , CM000666.1:g.12579920G>C GRCh37
NC_000004.10:g.12189018G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31046C>G
XR_001741374.1:n.254+44359C>G
XR_925406.3:n.140+31046C>G