Canonical Allele Identifier: CA410677499
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19711797G>C (hg19) chr22:g.19724274G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724274G>C , CM000684.2:g.19724274G>C GRCh38
NC_000022.10:g.19711797G>C , CM000684.1:g.19711797G>C GRCh37
NC_000022.9:g.18091797G>C NCBI36
NG_007974.1:g.5732G>C , LRG_478:g.5732G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.431G>C (GP1BB) MANE Select ENSP00000383382.2:p.Gly144Ala
ENST00000366425.3:c.431G>C (GP1BB) ENSP00000383382.2:p.Gly144Ala
ENST00000431044.5:c.*1516G>C (SEPTIN5) ENSP00000399685.1:n.*1516G>C
NM_000407.4:c.431G>C , LRG_478t1:c.431G>C (GP1BB) NP_000398.1:p.Gly144Ala
NR_037611.1:n.4171G>C
NR_037612.1:n.2675G>C
NM_000407.5:c.431G>C (GP1BB) MANE Select NP_000398.1:p.Gly144Ala
Search 100 bp 5'
Search 100 bp 3'