Canonical Allele Identifier: CA16841755
Gene:

Linked Data

dbSNP Id: rs987645384
gnomAD v3: 1-2036575-C-T
gnomAD v4: 1-2036575-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036575C>T , CM000663.2:g.2036575C>T GRCh38
NC_000001.10:g.1968014C>T , CM000663.1:g.1968014C>T GRCh37
NC_000001.9:g.1957874C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.633G>A
XR_001737845.2:n.636G>A
XR_946823.3:n.636G>A