Canonical Allele Identifier: CA2605563443
Gene:

Linked Data

dbSNP Id: rs2126848732

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748413A>G , CM000666.2:g.148748413A>G GRCh38
NC_000004.11:g.149669565A>G , CM000666.1:g.149669565A>G GRCh37
NC_000004.10:g.149889015A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741441.1:n.1746-118344A>G