Canonical Allele Identifier: CA615972261
Gene:

Linked Data

dbSNP Id: rs1375911285

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307374G>T , CM000676.2:g.92307374G>T GRCh38
NC_000014.8:g.92773718G>T , CM000676.1:g.92773718G>T GRCh37
NC_000014.7:g.91843471G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2830G>T