Canonical Allele Identifier: CA888766355

Gene:

Linked Data

• dbSNP Id: rs1358647178
• MyVariant Identifiers: chr1:g.147089050A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147089050A>G , CM000663.2:g.147089050A>G	GRCh38
NC_000001.10:g.146560597A>G , CM000663.1:g.146560597A>G	GRCh37
NC_000001.9:g.145027221A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000444082.1:n.1845+20812T>C