Canonical Allele Identifier: CA2619258002

Gene: RPS26

Linked Data

• gnomAD v4: 12-56041509-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041509G>T , CM000674.2:g.56041509G>T	GRCh38
NC_000012.11:g.56435293G>T , CM000674.1:g.56435293G>T	GRCh37
NC_000012.10:g.54721560G>T	NCBI36
NG_023201.1:g.4608G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+113G>T	ENSP00000348849.5:n.-357+113G>T
XR_944989.1:n.204C>A
XR_944990.1:n.204C>A
XR_944989.3:n.495C>A
XR_944990.3:n.495C>A