Canonical Allele Identifier: CA1458504718
Gene:

Linked Data

dbSNP Id: rs1720477849

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228370A>G , CM000666.2:g.54228370A>G GRCh38
NC_000004.11:g.55094537A>G , CM000666.1:g.55094537A>G GRCh37
NC_000004.10:g.54789294A>G NCBI36
NG_009250.1:g.4274A>G , LRG_309:g.4274A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46555A>G ENSP00000423325.1:n.1018-46555A>G