Canonical Allele Identifier: CA997753052
Gene:

Linked Data

dbSNP Id: rs1659182744
gnomAD v3: 1-2036486-G-T
gnomAD v4: 1-2036486-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036486G>T , CM000663.2:g.2036486G>T GRCh38
NC_000001.10:g.1967925G>T , CM000663.1:g.1967925G>T GRCh37
NC_000001.9:g.1957785G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.722C>A
XR_001737845.2:n.725C>A
XR_946823.3:n.725C>A