Canonical Allele Identifier: CA641901576

Gene: EBP

Linked Data

• dbSNP Id: rs1556977611
• gnomAD v2: X-48385696-G-T
• gnomAD v4: X-48527308-G-T
• MyVariant Identifiers: chrX:g.48385696G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527308G>T , CM000685.2:g.48527308G>T	GRCh38
NC_000023.10:g.48385696G>T , CM000685.1:g.48385696G>T	GRCh37
NC_000023.9:g.48270640G>T	NCBI36
NG_007452.1:g.10533G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.469+23G>T MANE Select	ENSP00000417052.1:n.469+23G>T
ENST00000651615.1:c.469+23G>T	ENSP00000498524.1:n.469+23G>T
ENST00000276096.10:n.427+23G>T
ENST00000446158.5:c.469+23G>T	ENSP00000390031.1:n.469+23G>T
ENST00000466461.1:n.331G>T
ENST00000495186.5:c.469+23G>T	ENSP00000417052.1:n.469+23G>T
ENST00000498425.1:n.590+23G>T
NM_006579.2:c.469+23G>T	NP_006570.1:n.469+23G>T
NM_006579.3:c.469+23G>T MANE Select	NP_006570.1:n.469+23G>T