Canonical Allele Identifier: CA410677631
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

gnomAD v4: 22-19724341-G-C
MyVariant Identifiers: chr22:g.19711864G>C (hg19) chr22:g.19724341G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724341G>C , CM000684.2:g.19724341G>C GRCh38
NC_000022.10:g.19711864G>C , CM000684.1:g.19711864G>C GRCh37
NC_000022.9:g.18091864G>C NCBI36
NG_007974.1:g.5799G>C , LRG_478:g.5799G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.498G>C (GP1BB) MANE Select ENSP00000383382.2:p.Leu166Phe
ENST00000366425.3:c.498G>C (GP1BB) ENSP00000383382.2:p.Leu166Phe
ENST00000431044.5:c.*1583G>C (SEPTIN5) ENSP00000399685.1:n.*1583G>C
NM_000407.4:c.498G>C , LRG_478t1:c.498G>C (GP1BB) NP_000398.1:p.Leu166Phe
NR_037611.1:n.4238G>C
NR_037612.1:n.2742G>C
NM_000407.5:c.498G>C (GP1BB) MANE Select NP_000398.1:p.Leu166Phe
Search 100 bp 5'
Search 100 bp 3'