Canonical Allele Identifier: CA1267947375
Gene:

Linked Data

dbSNP Id: rs1489047542
gnomAD v3: 2-88016195-T-C
gnomAD v4: 2-88016195-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016195T>C , CM000664.2:g.88016195T>C GRCh38
NC_000002.11:g.88315714T>C , CM000664.1:g.88315714T>C GRCh37
NC_000002.10:g.88096829T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.540T>C
XR_940336.3:n.540T>C