Canonical Allele Identifier: CA410677813
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19711962A>G (hg19) chr22:g.19724439A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724439A>G , CM000684.2:g.19724439A>G GRCh38
NC_000022.10:g.19711962A>G , CM000684.1:g.19711962A>G GRCh37
NC_000022.9:g.18091962A>G NCBI36
NG_007974.1:g.5897A>G , LRG_478:g.5897A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.596A>G (GP1BB) MANE Select ENSP00000383382.2:p.Glu199Gly
ENST00000366425.3:c.596A>G (GP1BB) ENSP00000383382.2:p.Glu199Gly
ENST00000431044.5:c.*1681A>G (SEPTIN5) ENSP00000399685.1:n.*1681A>G
NM_000407.4:c.596A>G , LRG_478t1:c.596A>G (GP1BB) NP_000398.1:p.Glu199Gly
NR_037611.1:n.4336A>G
NR_037612.1:n.2840A>G
NM_000407.5:c.596A>G (GP1BB) MANE Select NP_000398.1:p.Glu199Gly
Search 100 bp 5'
Search 100 bp 3'