Canonical Allele Identifier: CA34407256

Gene:

Linked Data

• dbSNP Id: rs1038072511
• gnomAD v4: 1-193121774-A-G
• MyVariant Identifiers: chr1:g.193121774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121774A>G , CM000663.2:g.193121774A>G	GRCh38
NC_000001.10:g.193090904A>G , CM000663.1:g.193090904A>G	GRCh37
NC_000001.9:g.191357527A>G	NCBI36
NG_012691.1:g.4817A>G , LRG_507:g.4817A>G

Transcript Alleles

HGVS	Amino-acid Change
XR_001738350.1:n.1883T>C