Canonical Allele Identifier: CA15451072

Gene:

Linked Data

• dbSNP Id: rs7772549
• gnomAD v2: 6-31407643-T-C
• gnomAD v3: 6-31439866-T-C
• gnomAD v4: 6-31439866-T-C
• MyVariant Identifiers: chr6:g.31407643T>C (hg19) ; chr6:g.31439866T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439866T>C , CM000668.2:g.31439866T>C	GRCh38
NC_000006.11:g.31407643T>C , CM000668.1:g.31407643T>C	GRCh37
NC_000006.10:g.31515622T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.241A>G