Canonical Allele Identifier: CA14772461
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs16985615

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661790T>C , CM000682.2:g.23661790T>C GRCh38
NC_000020.10:g.23642427T>C , CM000682.1:g.23642427T>C GRCh37
NC_000020.9:g.23590427T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+140T>C