Canonical Allele Identifier: CA200832984
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs2130014542
MyVariant Identifiers: chr9:g.133353790A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353790A>G , CM000671.2:g.133353790A>G GRCh38
NC_000009.10:g.135210466A>G NCBI36
NG_008477.1:g.7717T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.474T>C MANE Select ENSP00000361042.3:p.Ser158=
ENST00000371974.7:c.474T>C ENSP00000361042.3:p.Ser158=
ENST00000437995.1:n.420T>C
ENST00000495952.5:n.464T>C
ENST00000615505.4:c.147T>C ENSP00000482067.1:p.Ser49=
NM_001280787.1:c.147T>C NP_001267716.1:p.Ser49=
NM_003172.3:c.474T>C NP_003163.1:p.Ser158=
XM_011518942.1:c.147T>C XP_011517244.1:p.Ser49=
NM_003172.4:c.474T>C MANE Select NP_003163.1:p.Ser158=