Canonical Allele Identifier: CA2580574933
Gene:

Linked Data

dbSNP Id: rs2568958
gnomAD v3: 1-72299433-G-T
gnomAD v4: 1-72299433-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.72299433G>T , CM000663.2:g.72299433G>T GRCh38
NC_000001.10:g.72765116G>T , CM000663.1:g.72765116G>T GRCh37
NC_000001.9:g.72537704G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947505.1:n.310+16028G>T
XR_947506.1:n.310+16028G>T
XR_947507.1:n.310+16028G>T
XR_001737670.1:n.414+16028G>T
XR_001737671.2:n.418+16028G>T
XR_947505.2:n.414+16028G>T
XR_947506.2:n.414+16028G>T