Canonical Allele Identifier: CA1041166104

Gene:

Linked Data

• dbSNP Id: rs2077889342
• gnomAD v3: 2-200033258-A-C
• gnomAD v4: 2-200033258-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033258A>C , CM000664.2:g.200033258A>C	GRCh38
NC_000002.11:g.200897981A>C , CM000664.1:g.200897981A>C	GRCh37
NC_000002.10:g.200606226A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22362T>G