Canonical Allele Identifier: CA513686976
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

dbSNP Id: rs1285285577
MyVariant Identifiers: chr22:g.19711756C>G (hg19) chr22:g.19724233C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724233C>G , CM000684.2:g.19724233C>G GRCh38
NC_000022.10:g.19711756C>G , CM000684.1:g.19711756C>G GRCh37
NC_000022.9:g.18091756C>G NCBI36
NG_007974.1:g.5691C>G , LRG_478:g.5691C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.390C>G (GP1BB) MANE Select ENSP00000383382.2:p.Pro130=
ENST00000366425.3:c.390C>G (GP1BB) ENSP00000383382.2:p.Pro130=
ENST00000431044.5:c.*1475C>G (SEPTIN5) ENSP00000399685.1:n.*1475C>G
NM_000407.4:c.390C>G , LRG_478t1:c.390C>G (GP1BB) NP_000398.1:p.Pro130=
NR_037611.1:n.4130C>G
NR_037612.1:n.2634C>G
NM_000407.5:c.390C>G (GP1BB) MANE Select NP_000398.1:p.Pro130=
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