Canonical Allele Identifier: CA375693913
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs72619327
MyVariant Identifiers: chr9:g.133352593C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352593C>T , CM000671.2:g.133352593C>T GRCh38
NC_000009.10:g.135209269C>T NCBI36
NG_008477.1:g.8914G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.604G>A MANE Select ENSP00000361042.3:p.Asp202Asn
ENST00000371974.7:c.604G>A ENSP00000361042.3:p.Asp202Asn
ENST00000437995.1:n.514G>A
ENST00000495952.5:n.594G>A
ENST00000615505.4:c.277G>A ENSP00000482067.1:p.Asp93Asn
NM_001280787.1:c.277G>A NP_001267716.1:p.Asp93Asn
NM_003172.3:c.604G>A NP_003163.1:p.Asp202Asn
XM_011518942.1:c.277G>A XP_011517244.1:p.Asp93Asn
NM_003172.4:c.604G>A MANE Select NP_003163.1:p.Asp202Asn