Canonical Allele Identifier: CA1093891267
Gene:

Linked Data

dbSNP Id: rs9320841

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121793305A>T , CM000668.2:g.121793305A>T GRCh38
NC_000006.11:g.122114451A>T , CM000668.1:g.122114451A>T GRCh37
NC_000006.10:g.122156150A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942936.1:n.240+25690A>T
XR_942937.1:n.240+25690A>T
XR_942938.1:n.240+25690A>T
XR_942939.1:n.240+25690A>T
XR_942940.1:n.240+25690A>T
XR_942941.1:n.240+25690A>T
XR_942936.2:n.240+25690A>T
XR_942937.3:n.240+25690A>T