Canonical Allele Identifier: CA2711271373
Gene:

Linked Data

dbSNP Id: rs2113501140

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.23077032G>A , CM000668.2:g.23077032G>A GRCh38
NC_000006.11:g.23077260G>A , CM000668.1:g.23077260G>A GRCh37
NC_000006.10:g.23185239G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926583.1:n.246-19965C>T
XR_926584.1:n.246-60212C>T
XR_926583.2:n.246-19965C>T