Canonical Allele Identifier: CA1619157161

Gene:

Linked Data

• dbSNP Id: rs1761790948
• gnomAD v3: 6-31440028-A-C
• gnomAD v4: 6-31440028-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31440028A>C , CM000668.2:g.31440028A>C	GRCh38
NC_000006.11:g.31407805A>C , CM000668.1:g.31407805A>C	GRCh37
NC_000006.10:g.31515784A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.79T>G