Canonical Allele Identifier: CA860707704
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs376635181
MyVariant Identifiers: chr9:g.133352421C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352421C>G , CM000671.2:g.133352421C>G GRCh38
NC_000009.10:g.135209097C>G NCBI36
NG_008477.1:g.9086G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.751+25G>C MANE Select ENSP00000361042.3:n.751+25G>C
ENST00000371974.7:c.751+25G>C ENSP00000361042.3:n.751+25G>C
ENST00000437995.1:n.661+25G>C
ENST00000495952.5:n.741+25G>C
ENST00000615505.4:c.424+25G>C ENSP00000482067.1:n.424+25G>C
NM_001280787.1:c.424+25G>C NP_001267716.1:n.424+25G>C
NM_003172.3:c.751+25G>C NP_003163.1:n.751+25G>C
XM_011518942.1:c.424+25G>C XP_011517244.1:n.424+25G>C
NM_003172.4:c.751+25G>C MANE Select NP_003163.1:n.751+25G>C
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