Canonical Allele Identifier: CA1017753670
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs781665429

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460650A>G , CM000682.2:g.43460650A>G GRCh38
NC_000020.10:g.42089290A>G , CM000682.1:g.42089290A>G GRCh37
NC_000020.9:g.41522704A>G NCBI36
NG_029906.1:g.7787A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.675-53A>G MANE Select ENSP00000244020.3:n.675-53A>G
ENST00000657241.1:c.654+52A>G
ENST00000662078.1:c.674+52A>G ENSP00000499666.1:n.674+52A>G
ENST00000668808.1:c.675-53A>G ENSP00000499517.1:n.675-53A>G
ENST00000670741.1:c.674+52A>G ENSP00000499492.1:n.674+52A>G
ENST00000671022.1:n.765-53A>G
ENST00000244020.4:c.675-53A>G ENSP00000244020.3:n.675-53A>G
ENST00000483871.6:c.*535-53A>G ENSP00000433544.1:n.*535-53A>G
NM_006275.5:c.675-53A>G NP_006266.2:n.675-53A>G
NR_034009.1:n.1113-53A>G
XR_936608.1:n.1434-53A>G
XR_936608.2:n.1434-53A>G
NM_006275.6:c.675-53A>G MANE Select NP_006266.2:n.675-53A>G
NR_034009.2:n.1081-53A>G