Canonical Allele Identifier: CA375694215
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs1836497643
MyVariant Identifiers: chr9:g.133353795G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353795G>A , CM000671.2:g.133353795G>A GRCh38
NC_000009.10:g.135210471G>A NCBI36
NG_008477.1:g.7712C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.469C>T MANE Select ENSP00000361042.3:p.Gln157Ter
ENST00000371974.7:c.469C>T ENSP00000361042.3:p.Gln157Ter
ENST00000437995.1:n.415C>T
ENST00000495952.5:n.459C>T
ENST00000615505.4:c.142C>T ENSP00000482067.1:p.Gln48Ter
NM_001280787.1:c.142C>T NP_001267716.1:p.Gln48Ter
NM_003172.3:c.469C>T NP_003163.1:p.Gln157Ter
XM_011518942.1:c.142C>T XP_011517244.1:p.Gln48Ter
NM_003172.4:c.469C>T MANE Select NP_003163.1:p.Gln157Ter