Canonical Allele Identifier: CA2573144664

Gene:

Linked Data

• ClinVar Variation Id: 1525825
• ClinVar RCV Id: RCV002036978
• dbSNP Id: rs2131810512

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658046T>C , CM000671.2:g.35658046T>C	GRCh38
NC_000009.11:g.35658043T>C , CM000671.1:g.35658043T>C	GRCh37
NC_000009.10:g.35648043T>C	NCBI36
NG_017041.1:g.4973A>G , LRG_163:g.4973A>G
NG_033120.1:g.4757T>C