Canonical Allele Identifier: CA1035793767

Gene:

Linked Data

• gnomAD v3: 2-122369188-C-A
• gnomAD v4: 2-122369188-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122369188C>A , CM000664.2:g.122369188C>A	GRCh38
NC_000002.11:g.123126764C>A , CM000664.1:g.123126764C>A	GRCh37
NC_000002.10:g.122843234C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-23775C>A
XR_001739684.1:n.556-23775C>A