Canonical Allele Identifier: CA2655305008
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

gnomAD v4: 22-19723836-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19723836G>T , CM000684.2:g.19723836G>T GRCh38
NC_000022.10:g.19711359G>T , CM000684.1:g.19711359G>T GRCh37
NC_000022.9:g.18091359G>T NCBI36
NG_007974.1:g.5294G>T , LRG_478:g.5294G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.11-18G>T (GP1BB) MANE Select ENSP00000383382.2:n.11-18G>T
ENST00000366425.3:c.11-18G>T (GP1BB) ENSP00000383382.2:n.11-18G>T
ENST00000431044.5:c.*1096-18G>T (SEPTIN5) ENSP00000399685.1:n.*1096-18G>T
ENST00000455843.5:c.*1096-18G>T (SEPTIN5) ENSP00000391731.1:n.*1096-18G>T
ENST00000470814.1:n.1983-18G>T (SEPTIN5)
NM_000407.4:c.11-18G>T , LRG_478t1:c.11-18G>T (GP1BB) NP_000398.1:n.11-18G>T
NR_037611.1:n.3751-18G>T
NR_037612.1:n.2255-18G>T
NM_000407.5:c.11-18G>T (GP1BB) MANE Select NP_000398.1:n.11-18G>T
Search 100 bp 5'
Search 100 bp 3'