Canonical Allele Identifier: CA2667574578
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061520-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061520G>A , CM000665.2:g.129061520G>A GRCh38
NC_000003.11:g.128780363G>A , CM000665.1:g.128780363G>A GRCh37
NC_000003.10:g.130263053G>A NCBI36
NG_008715.1:g.5719G>A , LRG_477:g.5719G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-112G>A MANE Select ENSP00000303942.4:n.-112G>A
ENST00000307395.4:c.-112G>A ENSP00000303942.4:n.-112G>A
NM_000174.4:c.-112G>A , LRG_477t1:c.-112G>A NP_000165.1:n.-112G>A
XM_005247374.3:c.-112G>A XP_005247431.1:n.-112G>A
XM_011512701.1:c.-112G>A XP_011511003.1:n.-112G>A
XM_011512702.1:c.-12-208G>A XP_011511004.1:n.-12-208G>A
NM_000174.5:c.-112G>A MANE Select NP_000165.1:n.-112G>A
Search 100 bp 5'
Search 100 bp 3'