Canonical Allele Identifier: CA566344773

Gene:

Linked Data

• dbSNP Id: rs1157405499
• gnomAD v2: 6-31407849-G-A
• gnomAD v3: 6-31440072-G-A
• gnomAD v4: 6-31440072-G-A
• MyVariant Identifiers: chr6:g.31407849G>A (hg19) ; chr6:g.31440072G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31440072G>A , CM000668.2:g.31440072G>A	GRCh38
NC_000006.11:g.31407849G>A , CM000668.1:g.31407849G>A	GRCh37
NC_000006.10:g.31515828G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.55-20C>T