Canonical Allele Identifier: CA1619157172
Gene:

Linked Data

dbSNP Id: rs1761792326

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440050G>C , CM000668.2:g.31440050G>C GRCh38
NC_000006.11:g.31407827G>C , CM000668.1:g.31407827G>C GRCh37
NC_000006.10:g.31515806G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.57C>G