Canonical Allele Identifier: CA1087465207

Gene:

Linked Data

• dbSNP Id: rs1761774559
• gnomAD v3: 6-31439692-G-C
• gnomAD v4: 6-31439692-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439692G>C , CM000668.2:g.31439692G>C	GRCh38
NC_000006.11:g.31407469G>C , CM000668.1:g.31407469G>C	GRCh37
NC_000006.10:g.31515448G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.415C>G