Canonical Allele Identifier: CA731215520

Gene:

Linked Data

• dbSNP Id: rs1176456107
• MyVariant Identifiers: chr1:g.213855657A>G (hg19) ; chr1:g.213682314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.213682314A>G , CM000663.2:g.213682314A>G	GRCh38
NC_000001.10:g.213855657A>G , CM000663.1:g.213855657A>G	GRCh37
NC_000001.9:g.211922280A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738463.1:n.601-49103A>G
XR_001738464.1:n.426-49103A>G