Canonical Allele Identifier: CA41586377

Gene:

Linked Data

• dbSNP Id: rs573454645
• gnomAD v3: 2-773329-C-T
• gnomAD v4: 2-773329-C-T
• MyVariant Identifiers: chr2:g.773329C>T (hg19) ; chr2:g.773329C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.773329C>T , CM000664.2:g.773329C>T	GRCh38
NC_000002.11:g.773329C>T , CM000664.1:g.773329C>T	GRCh37
NC_000002.10:g.763329C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510439.1:c.-24-3507C>T	XP_011508741.1:n.-24-3507C>T
XM_011510440.1:c.-24-3507C>T	XP_011508742.1:n.-24-3507C>T
XM_011510441.1:c.-24-3507C>T	XP_011508743.1:n.-24-3507C>T
XM_011510442.1:c.-24-3507C>T	XP_011508744.1:n.-24-3507C>T
XM_011510443.1:c.-24-3507C>T	XP_011508745.1:n.-24-3507C>T
XR_922708.1:n.4001-3507C>T