Canonical Allele Identifier: CA9865224
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs781652566

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460732G>A , CM000682.2:g.43460732G>A GRCh38
NC_000020.10:g.42089372G>A , CM000682.1:g.42089372G>A GRCh37
NC_000020.9:g.41522786G>A NCBI36
NG_029906.1:g.7869G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.704G>A MANE Select ENSP00000244020.3:p.Arg235His
ENST00000657241.1:c.654+134G>A
ENST00000662078.1:c.674+134G>A ENSP00000499666.1:n.674+134G>A
ENST00000668808.1:c.704G>A ENSP00000499517.1:p.Arg235His
ENST00000670741.1:c.674+134G>A ENSP00000499492.1:n.674+134G>A
ENST00000671022.1:n.794G>A
ENST00000244020.4:c.704G>A ENSP00000244020.3:p.Arg235His
ENST00000483871.6:c.*564G>A ENSP00000433544.1:n.*564G>A
NM_006275.5:c.704G>A NP_006266.2:p.Arg235His
NR_034009.1:n.1142G>A
XR_936608.1:n.1463G>A
XR_936608.2:n.1463G>A
NM_006275.6:c.704G>A MANE Select NP_006266.2:p.Arg235His
NR_034009.2:n.1110G>A