Canonical Allele Identifier: CA36799059

Gene:

Linked Data

• dbSNP Id: rs945104892
• MyVariant Identifiers: chr1:g.211553144C>T (hg19) ; chr1:g.211379802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211379802C>T , CM000663.2:g.211379802C>T	GRCh38
NC_000001.10:g.211553144C>T , CM000663.1:g.211553144C>T	GRCh37
NC_000001.9:g.209619767C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738446.1:n.291+2393G>A