Canonical Allele Identifier: CA1033290816

Gene:

Linked Data

• dbSNP Id: rs1672671899
• gnomAD v3: 2-88016056-A-C
• gnomAD v4: 2-88016056-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016056A>C , CM000664.2:g.88016056A>C	GRCh38
NC_000002.11:g.88315575A>C , CM000664.1:g.88315575A>C	GRCh37
NC_000002.10:g.88096690A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.401A>C
XR_940336.3:n.401A>C