Canonical Allele Identifier: CA16956857

Gene:

Linked Data

• dbSNP Id: rs1020437691
• MyVariant Identifiers: chr1:g.2498881G>C (hg19) ; chr1:g.2567442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2567442G>C , CM000663.2:g.2567442G>C	GRCh38
NC_000001.10:g.2498881G>C , CM000663.1:g.2498881G>C	GRCh37
NC_000001.9:g.2475537C>G	NCBI36
NG_047096.1:g.16078G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_121638.1:n.71+837G>C