Canonical Allele Identifier: CA997753067
Gene:

Linked Data

dbSNP Id: rs1659184031
gnomAD v3: 1-2036565-C-T
gnomAD v4: 1-2036565-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036565C>T , CM000663.2:g.2036565C>T GRCh38
NC_000001.10:g.1968004C>T , CM000663.1:g.1968004C>T GRCh37
NC_000001.9:g.1957864C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.643G>A
XR_001737845.2:n.646G>A
XR_946823.3:n.646G>A