Canonical Allele Identifier: CA860709300
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs2130014646
MyVariant Identifiers: chr9:g.133353802G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353802G>A , CM000671.2:g.133353802G>A GRCh38
NC_000009.10:g.135210478G>A NCBI36
NG_008477.1:g.7705C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.462C>T MANE Select ENSP00000361042.3:p.Ser154=
ENST00000371974.7:c.462C>T ENSP00000361042.3:p.Ser154=
ENST00000437995.1:n.408C>T
ENST00000495952.5:n.452C>T
ENST00000615505.4:c.135C>T ENSP00000482067.1:p.Ser45=
NM_001280787.1:c.135C>T NP_001267716.1:p.Ser45=
NM_003172.3:c.462C>T NP_003163.1:p.Ser154=
XM_011518942.1:c.135C>T XP_011517244.1:p.Ser45=
NM_003172.4:c.462C>T MANE Select NP_003163.1:p.Ser154=