Canonical Allele Identifier: CA1033291237

Gene:

Linked Data

• dbSNP Id: rs183941072
• gnomAD v3: 2-88016291-T-C
• gnomAD v4: 2-88016291-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016291T>C , CM000664.2:g.88016291T>C	GRCh38
NC_000002.11:g.88315810T>C , CM000664.1:g.88315810T>C	GRCh37
NC_000002.10:g.88096925T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.636T>C
XR_940336.3:n.636T>C