Canonical Allele Identifier: CA566344754

Gene:

Linked Data

• dbSNP Id: rs1262301713
• gnomAD v2: 6-31407471-A-G
• gnomAD v3: 6-31439694-A-G
• gnomAD v4: 6-31439694-A-G
• MyVariant Identifiers: chr6:g.31407471A>G (hg19) ; chr6:g.31439694A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439694A>G , CM000668.2:g.31439694A>G	GRCh38
NC_000006.11:g.31407471A>G , CM000668.1:g.31407471A>G	GRCh37
NC_000006.10:g.31515450A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.413T>C