Canonical Allele Identifier: CA314557515

Gene: SRSF6

Linked Data

• dbSNP Id: rs368170771
• gnomAD v3: 20-43460789-A-T
• gnomAD v4: 20-43460789-A-T
• MyVariant Identifiers: chr20:g.42089429A>T (hg19) ; chr20:g.43460789A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460789A>T , CM000682.2:g.43460789A>T	GRCh38
NC_000020.10:g.42089429A>T , CM000682.1:g.42089429A>T	GRCh37
NC_000020.9:g.41522843A>T	NCBI36
NG_029906.1:g.7926A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.761A>T MANE Select	ENSP00000244020.3:p.Asp254Val
ENST00000657241.1:c.654+191A>T
ENST00000662078.1:c.674+191A>T	ENSP00000499666.1:n.674+191A>T
ENST00000668808.1:c.761A>T	ENSP00000499517.1:p.Asp254Val
ENST00000670741.1:c.674+191A>T	ENSP00000499492.1:n.674+191A>T
ENST00000671022.1:n.851A>T
ENST00000244020.4:c.761A>T	ENSP00000244020.3:p.Asp254Val
ENST00000483871.6:c.*621A>T	ENSP00000433544.1:n.*621A>T
NM_006275.5:c.761A>T	NP_006266.2:p.Asp254Val
NR_034009.1:n.1199A>T
XR_936608.1:n.1520A>T
XR_936608.2:n.1520A>T
NM_006275.6:c.761A>T MANE Select	NP_006266.2:p.Asp254Val
NR_034009.2:n.1167A>T