Canonical Allele Identifier: CA375694211
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133353793C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353793C>G , CM000671.2:g.133353793C>G GRCh38
NC_000009.10:g.135210469C>G NCBI36
NG_008477.1:g.7714G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.471G>C MANE Select ENSP00000361042.3:p.Gln157His
ENST00000371974.7:c.471G>C ENSP00000361042.3:p.Gln157His
ENST00000437995.1:n.417G>C
ENST00000495952.5:n.461G>C
ENST00000615505.4:c.144G>C ENSP00000482067.1:p.Gln48His
NM_001280787.1:c.144G>C NP_001267716.1:p.Gln48His
NM_003172.3:c.471G>C NP_003163.1:p.Gln157His
XM_011518942.1:c.144G>C XP_011517244.1:p.Gln48His
NM_003172.4:c.471G>C MANE Select NP_003163.1:p.Gln157His
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