Canonical Allele Identifier: CA15478076

Gene:

Linked Data

• dbSNP Id: rs2844520
• gnomAD v2: 6-31407758-G-T
• gnomAD v3: 6-31439981-G-T
• gnomAD v4: 6-31439981-G-T
• MyVariant Identifiers: chr6:g.31407758G>T (hg19) ; chr6:g.31439981G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439981G>T , CM000668.2:g.31439981G>T	GRCh38
NC_000006.11:g.31407758G>T , CM000668.1:g.31407758G>T	GRCh37
NC_000006.10:g.31515737G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_926694.1:n.126C>A