Canonical Allele Identifier: CA409071921

Gene: SRSF6

Linked Data

• dbSNP Id: rs756216686
• gnomAD v3: 20-43460887-G-C
• gnomAD v4: 20-43460887-G-C
• MyVariant Identifiers: chr20:g.42089527G>C (hg19) ; chr20:g.43460887G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.859G>C MANE Select	ENSP00000244020.3:p.Gly287Arg
ENST00000657241.1:c.654+289G>C
ENST00000662078.1:c.674+289G>C	ENSP00000499666.1:n.674+289G>C
ENST00000668808.1:c.824+35G>C	ENSP00000499517.1:n.824+35G>C
ENST00000670741.1:c.674+289G>C	ENSP00000499492.1:n.674+289G>C
ENST00000671022.1:n.949G>C
ENST00000244020.4:c.859G>C	ENSP00000244020.3:p.Gly287Arg
ENST00000483871.6:c.*719G>C	ENSP00000433544.1:n.*719G>C
NM_006275.5:c.859G>C	NP_006266.2:p.Gly287Arg
NR_034009.1:n.1297G>C
XR_936608.2:n.1618G>C
NM_006275.6:c.859G>C MANE Select	NP_006266.2:p.Gly287Arg
NR_034009.2:n.1265G>C