Canonical Allele Identifier: CA1619157060
Gene:

Linked Data

dbSNP Id: rs549791443

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439751G>T , CM000668.2:g.31439751G>T GRCh38
NC_000006.11:g.31407528G>T , CM000668.1:g.31407528G>T GRCh37
NC_000006.10:g.31515507G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.356C>A