Canonical Allele Identifier: CA54965472
Gene:

Linked Data

dbSNP Id: rs1028508491

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368862A>T , CM000664.2:g.122368862A>T GRCh38
NC_000002.11:g.123126438A>T , CM000664.1:g.123126438A>T GRCh37
NC_000002.10:g.122842908A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24101A>T
XR_001739684.1:n.556-24101A>T