Canonical Allele Identifier: CA842011401
Gene: BUD23 HGNC NCBI

Linked Data

dbSNP Id: rs1203846675
gnomAD v3: 7-73683572-T-G
gnomAD v4: 7-73683572-T-G
MyVariant Identifiers: chr7:g.73683572T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73683572T>G , CM000669.2:g.73683572T>G GRCh38
NC_000007.13:g.73097902T>G , CM000669.1:g.73097902T>G GRCh37
NC_000007.12:g.72735838T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265758.6:c.-54T>G ENSP00000265758.2:n.-54T>G
ENST00000421304.5:c.-266T>G ENSP00000391761.2:n.-266T>G
ENST00000432522.5:c.-54T>G ENSP00000390136.1:n.-54T>G
ENST00000464615.1:n.359+189T>G
NM_001202560.2:c.-54T>G NP_001189489.1:n.-54T>G
NM_017528.4:c.-54T>G NP_059998.2:n.-54T>G
NR_037776.2:n.5T>G
NR_045512.1:n.5T>G
XM_006715847.1:c.-82T>G XP_006715910.1:n.-82T>G
XM_011515778.1:c.-82T>G XP_011514080.1:n.-82T>G
XM_011515779.1:c.-54T>G XP_011514081.1:n.-54T>G
XR_927349.1:n.7T>G
XR_927350.1:n.7T>G
XM_011515779.2:c.-54T>G XP_011514081.1:n.-54T>G
XR_002956407.1:n.2T>G