Canonical Allele Identifier: CA2649624179

Gene:

Linked Data

• dbSNP Id: rs2103110536
• gnomAD v4: 1-193121697-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121697G>A , CM000663.2:g.193121697G>A	GRCh38
NC_000001.10:g.193090827G>A , CM000663.1:g.193090827G>A	GRCh37
NC_000001.9:g.191357450G>A	NCBI36
NG_012691.1:g.4740G>A , LRG_507:g.4740G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_001738350.1:n.1960C>T