Canonical Allele Identifier: CA575783403

Gene: BUD23

Linked Data

• dbSNP Id: rs1554611970
• gnomAD v2: 7-73097911-G-C
• MyVariant Identifiers: chr7:g.73097911G>C (hg19) ; chr7:g.73683581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73683581G>C , CM000669.2:g.73683581G>C	GRCh38
NC_000007.13:g.73097911G>C , CM000669.1:g.73097911G>C	GRCh37
NC_000007.12:g.72735847G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265758.6:c.-45G>C	ENSP00000265758.2:n.-45G>C
ENST00000421304.5:c.-257G>C	ENSP00000391761.2:n.-257G>C
ENST00000421744.5:c.-45G>C	ENSP00000404981.1:n.-45G>C
ENST00000432522.5:c.-45G>C	ENSP00000390136.1:n.-45G>C
ENST00000464615.1:n.359+198G>C
NM_001202560.2:c.-45G>C	NP_001189489.1:n.-45G>C
NM_017528.4:c.-45G>C	NP_059998.2:n.-45G>C
NR_037776.2:n.14G>C
NR_045512.1:n.14G>C
XM_006715847.1:c.-73G>C	XP_006715910.1:n.-73G>C
XM_011515778.1:c.-73G>C	XP_011514080.1:n.-73G>C
XM_011515779.1:c.-45G>C	XP_011514081.1:n.-45G>C
XR_927349.1:n.16G>C
XR_927350.1:n.16G>C
XM_011515779.2:c.-45G>C	XP_011514081.1:n.-45G>C
XR_002956407.1:n.11G>C