Canonical Allele Identifier: CA1216113165

Gene:

Linked Data

• dbSNP Id: rs1675450484
• gnomAD v4: 1-193121832-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121832C>G , CM000663.2:g.193121832C>G	GRCh38
NC_000001.10:g.193090962C>G , CM000663.1:g.193090962C>G	GRCh37
NC_000001.9:g.191357585C>G	NCBI36
NG_012691.1:g.4875C>G , LRG_507:g.4875C>G

Transcript Alleles

HGVS	Amino-acid Change
XR_001738350.1:n.1825G>C