Canonical Allele Identifier: CA566344769

Gene:

Linked Data

• dbSNP Id: rs1289258743
• gnomAD v2: 6-31407741-A-G
• gnomAD v3: 6-31439964-A-G
• gnomAD v4: 6-31439964-A-G
• MyVariant Identifiers: chr6:g.31407741A>G (hg19) ; chr6:g.31439964A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439964A>G , CM000668.2:g.31439964A>G	GRCh38
NC_000006.11:g.31407741A>G , CM000668.1:g.31407741A>G	GRCh37
NC_000006.10:g.31515720A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.143T>C