Canonical Allele Identifier: CA566344752

Gene:

Linked Data

• dbSNP Id: rs1219938889
• gnomAD v2: 6-31407421-T-C
• gnomAD v3: 6-31439644-T-C
• gnomAD v4: 6-31439644-T-C
• MyVariant Identifiers: chr6:g.31407421T>C (hg19) ; chr6:g.31439644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439644T>C , CM000668.2:g.31439644T>C	GRCh38
NC_000006.11:g.31407421T>C , CM000668.1:g.31407421T>C	GRCh37
NC_000006.10:g.31515400T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.463A>G