Canonical Allele Identifier: CA638352884
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

dbSNP Id: rs1257960444
gnomAD v2: 22-19711997-C-T
gnomAD v3: 22-19724474-C-T
gnomAD v4: 22-19724474-C-T
MyVariant Identifiers: chr22:g.19711997C>T (hg19) chr22:g.19724474C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724474C>T , CM000684.2:g.19724474C>T GRCh38
NC_000022.10:g.19711997C>T , CM000684.1:g.19711997C>T GRCh37
NC_000022.9:g.18091997C>T NCBI36
NG_007974.1:g.5932C>T , LRG_478:g.5932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.*10C>T (GP1BB) MANE Select ENSP00000383382.2:n.*10C>T
ENST00000366425.3:c.*10C>T (GP1BB) ENSP00000383382.2:n.*10C>T
ENST00000431044.5:c.*1716C>T (SEPTIN5) ENSP00000399685.1:n.*1716C>T
NM_000407.4:c.*10C>T , LRG_478t1:c.*10C>T (GP1BB) NP_000398.1:n.*10C>T
NR_037611.1:n.4371C>T
NR_037612.1:n.2875C>T
NM_000407.5:c.*10C>T (GP1BB) MANE Select NP_000398.1:n.*10C>T
Search 100 bp 5'
Search 100 bp 3'