Canonical Allele Identifier: CA2184016
Gene: SH3BP4 HGNC NCBI

Linked Data

dbSNP Id: rs749330482

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.235052604A>G , CM000664.2:g.235052604A>G GRCh38
NC_000002.11:g.235961248A>G , CM000664.1:g.235961248A>G GRCh37
NC_000002.10:g.235625987A>G NCBI36
NG_033930.1:g.105621A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392011.7:c.2521A>G MANE Select ENSP00000375867.2:p.Ile841Val
ENST00000344528.8:c.2521A>G ENSP00000340237.4:p.Ile841Val
ENST00000392011.6:c.2521A>G ENSP00000375867.2:p.Ile841Val
ENST00000409212.5:c.2521A>G ENSP00000386862.1:p.Ile841Val
NM_014521.2:c.2521A>G NP_055336.1:p.Ile841Val
XM_011510891.1:c.2521A>G XP_011509193.1:p.Ile841Val
XM_011510892.1:c.2521A>G XP_011509194.1:p.Ile841Val
XM_011510893.1:c.2521A>G XP_011509195.1:p.Ile841Val
XM_011510894.1:c.2521A>G XP_011509196.1:p.Ile841Val
XM_011510891.2:c.2521A>G XP_011509193.1:p.Ile841Val
XM_011510894.2:c.2521A>G XP_011509196.1:p.Ile841Val
NM_014521.3:c.2521A>G MANE Select NP_055336.1:p.Ile841Val
NM_001371302.1:c.2521A>G NP_001358231.1:p.Ile841Val
NM_001371303.1:c.2521A>G NP_001358232.1:p.Ile841Val
NM_001371304.1:c.2521A>G NP_001358233.1:p.Ile841Val
NM_001371305.1:c.2521A>G NP_001358234.1:p.Ile841Val
NM_001371306.1:c.2521A>G NP_001358235.1:p.Ile841Val