Canonical Allele Identifier: CA1595159040
Gene:

Linked Data

dbSNP Id: rs1757450462

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580693G>T , CM000667.2:g.159580693G>T GRCh38
NC_000005.9:g.159007701G>T , CM000667.1:g.159007701G>T GRCh37
NC_000005.8:g.158940279G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+258G>T
XR_941140.1:n.2075+258G>T
XR_941141.1:n.570+258G>T
XR_941139.2:n.2229+258G>T