Canonical Allele Identifier: CA136858924

Gene:

Linked Data

• dbSNP Id: rs549791443
• gnomAD v3: 6-31439751-G-A
• gnomAD v4: 6-31439751-G-A
• MyVariant Identifiers: chr6:g.31407528G>A (hg19) ; chr6:g.31439751G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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