Canonical Allele Identifier: CA513686868
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19711627C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724104C>A , CM000684.2:g.19724104C>A GRCh38
NC_000022.10:g.19711627C>A , CM000684.1:g.19711627C>A GRCh37
NC_000022.9:g.18091627C>A NCBI36
NG_007974.1:g.5562C>A , LRG_478:g.5562C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.261C>A (GP1BB) MANE Select ENSP00000383382.2:p.Gly87=
ENST00000366425.3:c.261C>A (GP1BB) ENSP00000383382.2:p.Gly87=
ENST00000431044.5:c.*1346C>A (SEPTIN5) ENSP00000399685.1:n.*1346C>A
ENST00000455843.5:c.*1346C>A (SEPTIN5) ENSP00000391731.1:n.*1346C>A
ENST00000470814.1:n.2233C>A (SEPTIN5)
NM_000407.4:c.261C>A , LRG_478t1:c.261C>A (GP1BB) NP_000398.1:p.Gly87=
NR_037611.1:n.4001C>A
NR_037612.1:n.2505C>A
NM_000407.5:c.261C>A (GP1BB) MANE Select NP_000398.1:p.Gly87=
Search 100 bp 5'
Search 100 bp 3'