Canonical Allele Identifier: CA1095144124
Gene:

Linked Data

dbSNP Id: rs1775186536

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.140848712A>G , CM000668.2:g.140848712A>G GRCh38
NC_000006.11:g.141169849A>G , CM000668.1:g.141169849A>G GRCh37
NC_000006.10:g.141211542A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428030.2:n.327-2408T>C
XR_943075.1:n.315-2408T>C
XR_943076.1:n.246-2408T>C
XR_001744390.1:n.235-32482T>C
XR_428030.4:n.341-2408T>C
XR_943075.3:n.329-2408T>C