Canonical Allele Identifier: CA51878297
Gene:

Linked Data

dbSNP Id: rs1045972638
gnomAD v2: 2-88315713-G-C
gnomAD v3: 2-88016194-G-C
gnomAD v4: 2-88016194-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016194G>C , CM000664.2:g.88016194G>C GRCh38
NC_000002.11:g.88315713G>C , CM000664.1:g.88315713G>C GRCh37
NC_000002.10:g.88096828G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.539G>C
XR_940336.3:n.539G>C