Canonical Allele Identifier: CA410677052
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19711659T>A (hg19) chr22:g.19724136T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724136T>A , CM000684.2:g.19724136T>A GRCh38
NC_000022.10:g.19711659T>A , CM000684.1:g.19711659T>A GRCh37
NC_000022.9:g.18091659T>A NCBI36
NG_007974.1:g.5594T>A , LRG_478:g.5594T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.293T>A (GP1BB) MANE Select ENSP00000383382.2:p.Val98Glu
ENST00000366425.3:c.293T>A (GP1BB) ENSP00000383382.2:p.Val98Glu
ENST00000431044.5:c.*1378T>A (SEPTIN5) ENSP00000399685.1:n.*1378T>A
ENST00000455843.5:c.*1378T>A (SEPTIN5) ENSP00000391731.1:n.*1378T>A
ENST00000470814.1:n.2265T>A (SEPTIN5)
NM_000407.4:c.293T>A , LRG_478t1:c.293T>A (GP1BB) NP_000398.1:p.Val98Glu
NR_037611.1:n.4033T>A
NR_037612.1:n.2537T>A
NM_000407.5:c.293T>A (GP1BB) MANE Select NP_000398.1:p.Val98Glu
Search 100 bp 5'
Search 100 bp 3'