Canonical Allele Identifier: CA598391614

Gene: FSHB ARL14EP-DT

Linked Data

• dbSNP Id: rs1346869825
• gnomAD v2: 11-30255108-A-G
• gnomAD v4: 11-30233561-A-G
• MyVariant Identifiers: chr11:g.30255108A>G (hg19) ; chr11:g.30233561A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.30233561A>G , CM000673.2:g.30233561A>G	GRCh38
NC_000011.9:g.30255108A>G , CM000673.1:g.30255108A>G	GRCh37
NC_000011.8:g.30211684A>G	NCBI36
NG_008144.1:g.7546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254122.8:c.160-9A>G (FSHB)	ENSP00000254122.3:n.160-9A>G
ENST00000533718.2:c.160-9A>G (FSHB) MANE Select	ENSP00000433424.1:n.160-9A>G
ENST00000254122.7:c.160-9A>G (FSHB)	ENSP00000254122.3:n.160-9A>G
ENST00000417547.1:c.160-9A>G (FSHB)	ENSP00000416606.1:n.160-9A>G
ENST00000533718.1:c.160-9A>G (FSHB)	ENSP00000433424.1:n.160-9A>G
NM_000510.2:c.160-9A>G (FSHB)	NP_000501.1:n.160-9A>G
NM_001018080.1:c.160-9A>G (FSHB)	NP_001018090.1:n.160-9A>G
XM_011519964.1:c.160-9A>G (FSHB)	XP_011518266.1:n.160-9A>G
XR_931152.1:n.463+83329T>C (ARL14EP-DT)
XR_931153.1:n.284+83329T>C (ARL14EP-DT)
XR_931152.2:n.463+83329T>C (ARL14EP-DT)
NM_000510.3:c.160-9A>G (FSHB)	NP_000501.1:n.160-9A>G
NM_001018080.2:c.160-9A>G (FSHB)	NP_001018090.1:n.160-9A>G
NM_000510.4:c.160-9A>G (FSHB)	NP_000501.1:n.160-9A>G
NM_001018080.3:c.160-9A>G (FSHB)	NP_001018090.1:n.160-9A>G
NM_001382289.1:c.160-9A>G (FSHB) MANE Select	NP_001369218.1:n.160-9A>G