Canonical Allele Identifier: CA936776395
Gene:

Linked Data

dbSNP Id: rs1696614288

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759462G>T , CM000673.2:g.34759462G>T GRCh38
NC_000011.9:g.34781009G>T , CM000673.1:g.34781009G>T GRCh37
NC_000011.8:g.34737585G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4855G>T
XR_931188.1:n.693+4855G>T
XR_931189.1:n.854+4855G>T
XR_931190.1:n.639+4855G>T
XR_931191.1:n.689+4855G>T
XR_001748174.1:n.855+4855G>T
XR_001748176.1:n.1016+4855G>T
XR_002957246.1:n.639+4855G>T