Canonical Allele Identifier: CA9865261
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs756216686

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460887G>A , CM000682.2:g.43460887G>A GRCh38
NC_000020.10:g.42089527G>A , CM000682.1:g.42089527G>A GRCh37
NC_000020.9:g.41522941G>A NCBI36
NG_029906.1:g.8024G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.859G>A MANE Select ENSP00000244020.3:p.Gly287Ser
ENST00000657241.1:c.654+289G>A
ENST00000662078.1:c.674+289G>A ENSP00000499666.1:n.674+289G>A
ENST00000668808.1:c.824+35G>A ENSP00000499517.1:n.824+35G>A
ENST00000670741.1:c.674+289G>A ENSP00000499492.1:n.674+289G>A
ENST00000671022.1:n.949G>A
ENST00000244020.4:c.859G>A ENSP00000244020.3:p.Gly287Ser
ENST00000483871.6:c.*719G>A ENSP00000433544.1:n.*719G>A
NM_006275.5:c.859G>A NP_006266.2:p.Gly287Ser
NR_034009.1:n.1297G>A
XR_936608.2:n.1618G>A
NM_006275.6:c.859G>A MANE Select NP_006266.2:p.Gly287Ser
NR_034009.2:n.1265G>A