Canonical Allele Identifier: CA351164775

Gene: SH3BP4

Linked Data

• MyVariant Identifiers: chr2:g.235961209C>G (hg19) ; chr2:g.235052565C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.235052565C>G , CM000664.2:g.235052565C>G	GRCh38
NC_000002.11:g.235961209C>G , CM000664.1:g.235961209C>G	GRCh37
NC_000002.10:g.235625948C>G	NCBI36
NG_033930.1:g.105582C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392011.7:c.2482C>G MANE Select	ENSP00000375867.2:p.Leu828Val
ENST00000344528.8:c.2482C>G	ENSP00000340237.4:p.Leu828Val
ENST00000392011.6:c.2482C>G	ENSP00000375867.2:p.Leu828Val
ENST00000409212.5:c.2482C>G	ENSP00000386862.1:p.Leu828Val
NM_014521.2:c.2482C>G	NP_055336.1:p.Leu828Val
XM_011510891.1:c.2482C>G	XP_011509193.1:p.Leu828Val
XM_011510892.1:c.2482C>G	XP_011509194.1:p.Leu828Val
XM_011510893.1:c.2482C>G	XP_011509195.1:p.Leu828Val
XM_011510894.1:c.2482C>G	XP_011509196.1:p.Leu828Val
XM_011510891.2:c.2482C>G	XP_011509193.1:p.Leu828Val
XM_011510894.2:c.2482C>G	XP_011509196.1:p.Leu828Val
NM_014521.3:c.2482C>G MANE Select	NP_055336.1:p.Leu828Val
NM_001371302.1:c.2482C>G	NP_001358231.1:p.Leu828Val
NM_001371303.1:c.2482C>G	NP_001358232.1:p.Leu828Val
NM_001371304.1:c.2482C>G	NP_001358233.1:p.Leu828Val
NM_001371305.1:c.2482C>G	NP_001358234.1:p.Leu828Val
NM_001371306.1:c.2482C>G	NP_001358235.1:p.Leu828Val