Canonical Allele Identifier: CA756174381
Gene:

Linked Data

dbSNP Id: rs1209065413

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368962A>G , CM000664.2:g.122368962A>G GRCh38
NC_000002.11:g.123126538A>G , CM000664.1:g.123126538A>G GRCh37
NC_000002.10:g.122843008A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24001A>G
XR_001739684.1:n.556-24001A>G