Canonical Allele Identifier: CA2341104172
Gene:

Linked Data

dbSNP Id: rs1599971042

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837451A>C , CM000681.2:g.50837451A>C GRCh38
NC_000019.9:g.51340707A>C , CM000681.1:g.51340707A>C GRCh37
NC_000019.8:g.56032519A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6158A>C
NR_131205.1:n.230+6158A>C
XR_936030.1:n.298+6158A>C
XR_936031.1:n.298+6158A>C
XR_936032.1:n.298+6158A>C
XR_936033.1:n.294+6158A>C
XR_936035.1:n.281+6158A>C