Canonical Allele Identifier: CA513687002
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

gnomAD v4: 22-19724269-T-C
MyVariant Identifiers: chr22:g.19711792T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724269T>C , CM000684.2:g.19724269T>C GRCh38
NC_000022.10:g.19711792T>C , CM000684.1:g.19711792T>C GRCh37
NC_000022.9:g.18091792T>C NCBI36
NG_007974.1:g.5727T>C , LRG_478:g.5727T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.426T>C (GP1BB) MANE Select ENSP00000383382.2:p.Ala142=
ENST00000366425.3:c.426T>C (GP1BB) ENSP00000383382.2:p.Ala142=
ENST00000431044.5:c.*1511T>C (SEPTIN5) ENSP00000399685.1:n.*1511T>C
NM_000407.4:c.426T>C , LRG_478t1:c.426T>C (GP1BB) NP_000398.1:p.Ala142=
NR_037611.1:n.4166T>C
NR_037612.1:n.2670T>C
NM_000407.5:c.426T>C (GP1BB) MANE Select NP_000398.1:p.Ala142=
Search 100 bp 5'
Search 100 bp 3'