Canonical Allele Identifier: CA107997237
Gene:

Linked Data

dbSNP Id: rs910863538

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748258A>G , CM000666.2:g.148748258A>G GRCh38
NC_000004.11:g.149669410A>G , CM000666.1:g.149669410A>G GRCh37
NC_000004.10:g.149888860A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118499A>G