Canonical Allele Identifier: CA914614997
Gene: SRSF6 HGNC NCBI

Linked Data

dbSNP Id: rs1568900874

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460657G>A , CM000682.2:g.43460657G>A GRCh38
NC_000020.10:g.42089297G>A , CM000682.1:g.42089297G>A GRCh37
NC_000020.9:g.41522711G>A NCBI36
NG_029906.1:g.7794G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.675-46G>A MANE Select ENSP00000244020.3:n.675-46G>A
ENST00000657241.1:c.654+59G>A
ENST00000662078.1:c.674+59G>A ENSP00000499666.1:n.674+59G>A
ENST00000668808.1:c.675-46G>A ENSP00000499517.1:n.675-46G>A
ENST00000670741.1:c.674+59G>A ENSP00000499492.1:n.674+59G>A
ENST00000671022.1:n.765-46G>A
ENST00000244020.4:c.675-46G>A ENSP00000244020.3:n.675-46G>A
ENST00000483871.6:c.*535-46G>A ENSP00000433544.1:n.*535-46G>A
NM_006275.5:c.675-46G>A NP_006266.2:n.675-46G>A
NR_034009.1:n.1113-46G>A
XR_936608.1:n.1434-46G>A
XR_936608.2:n.1434-46G>A
NM_006275.6:c.675-46G>A MANE Select NP_006266.2:n.675-46G>A
NR_034009.2:n.1081-46G>A