Canonical Allele Identifier: CA1468682059
Gene:

Linked Data

dbSNP Id: rs10027097

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553977A>C , CM000666.2:g.74553977A>C GRCh38
NC_000004.11:g.75419694A>C , CM000666.1:g.75419694A>C GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1145T>G