Canonical Allele Identifier: CA860707707
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs368743250
MyVariant Identifiers: chr9:g.133352422G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352422G>C , CM000671.2:g.133352422G>C GRCh38
NC_000009.10:g.135209098G>C NCBI36
NG_008477.1:g.9085C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.751+24C>G MANE Select ENSP00000361042.3:n.751+24C>G
ENST00000371974.7:c.751+24C>G ENSP00000361042.3:n.751+24C>G
ENST00000437995.1:n.661+24C>G
ENST00000495952.5:n.741+24C>G
ENST00000615505.4:c.424+24C>G ENSP00000482067.1:n.424+24C>G
NM_001280787.1:c.424+24C>G NP_001267716.1:n.424+24C>G
NM_003172.3:c.751+24C>G NP_003163.1:n.751+24C>G
XM_011518942.1:c.424+24C>G XP_011517244.1:n.424+24C>G
NM_003172.4:c.751+24C>G MANE Select NP_003163.1:n.751+24C>G