Canonical Allele Identifier: CA1691656431
Gene:

Linked Data

dbSNP Id: rs375290849

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957828G>C , CM000669.2:g.17957828G>C GRCh38
NC_000007.13:g.17997451G>C , CM000669.1:g.17997451G>C GRCh37
NC_000007.12:g.17963976G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-842G>C