Canonical Allele Identifier: CA64382904

Gene:

Linked Data

• dbSNP Id: rs953330891
• gnomAD v3: 2-200033211-C-T
• gnomAD v4: 2-200033211-C-T
• MyVariant Identifiers: chr2:g.200033211C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033211C>T , CM000664.2:g.200033211C>T	GRCh38
NC_000002.11:g.200897934C>T , CM000664.1:g.200897934C>T	GRCh37
NC_000002.10:g.200606179C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22315G>A