Canonical Allele Identifier: CA1216113166

Gene:

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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