Canonical Allele Identifier: CA35069260
Gene:

Linked Data

dbSNP Id: rs190193317

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800600A>C , CM000663.2:g.192800600A>C GRCh38
NC_000001.10:g.192769730A>C , CM000663.1:g.192769730A>C GRCh37
NC_000001.9:g.191036353A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.30A>C