Canonical Allele Identifier: CA354447330
Gene: GP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.128780775T>A (hg19) chr3:g.129061932T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061932T>A , CM000665.2:g.129061932T>A GRCh38
NC_000003.11:g.128780775T>A , CM000665.1:g.128780775T>A GRCh37
NC_000003.10:g.130263465T>A NCBI36
NG_008715.1:g.6131T>A , LRG_477:g.6131T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.193T>A MANE Select ENSP00000303942.4:p.Ser65Thr
ENST00000307395.4:c.193T>A ENSP00000303942.4:p.Ser65Thr
NM_000174.4:c.193T>A , LRG_477t1:c.193T>A NP_000165.1:p.Ser65Thr
XM_005247374.3:c.193T>A XP_005247431.1:p.Ser65Thr
XM_011512701.1:c.193T>A XP_011511003.1:p.Ser65Thr
XM_011512702.1:c.193T>A XP_011511004.1:p.Ser65Thr
NM_000174.5:c.193T>A MANE Select NP_000165.1:p.Ser65Thr
Search 100 bp 5'
Search 100 bp 3'