Canonical Allele Identifier: CA2736862903
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs1568900906

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460667A>C , CM000682.2:g.43460667A>C GRCh38
NC_000020.10:g.42089307A>C , CM000682.1:g.42089307A>C GRCh37
NC_000020.9:g.41522721A>C NCBI36
NG_029906.1:g.7804A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.675-36A>C MANE Select ENSP00000244020.3:n.675-36A>C
ENST00000657241.1:c.654+69A>C
ENST00000662078.1:c.674+69A>C ENSP00000499666.1:n.674+69A>C
ENST00000668808.1:c.675-36A>C ENSP00000499517.1:n.675-36A>C
ENST00000670741.1:c.674+69A>C ENSP00000499492.1:n.674+69A>C
ENST00000671022.1:n.765-36A>C
ENST00000244020.4:c.675-36A>C ENSP00000244020.3:n.675-36A>C
ENST00000483871.6:c.*535-36A>C ENSP00000433544.1:n.*535-36A>C
NM_006275.5:c.675-36A>C NP_006266.2:n.675-36A>C
NR_034009.1:n.1113-36A>C
XR_936608.1:n.1434-36A>C
XR_936608.2:n.1434-36A>C
NM_006275.6:c.675-36A>C MANE Select NP_006266.2:n.675-36A>C
NR_034009.2:n.1081-36A>C