Canonical Allele Identifier: CA1336501380

Gene: SH3BP4

Linked Data

• dbSNP Id: rs879783028

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.235052190C>T , CM000664.2:g.235052190C>T	GRCh38
NC_000002.11:g.235960834C>T , CM000664.1:g.235960834C>T	GRCh37
NC_000002.10:g.235625573C>T	NCBI36
NG_033930.1:g.105207C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000392011.7:c.2479-372C>T MANE Select	ENSP00000375867.2:n.2479-372C>T
ENST00000344528.8:c.2479-372C>T	ENSP00000340237.4:n.2479-372C>T
ENST00000392011.6:c.2479-372C>T	ENSP00000375867.2:n.2479-372C>T
ENST00000409212.5:c.2479-372C>T	ENSP00000386862.1:n.2479-372C>T
NM_014521.2:c.2479-372C>T	NP_055336.1:n.2479-372C>T
XM_011510891.1:c.2479-372C>T	XP_011509193.1:n.2479-372C>T
XM_011510892.1:c.2479-372C>T	XP_011509194.1:n.2479-372C>T
XM_011510893.1:c.2479-372C>T	XP_011509195.1:n.2479-372C>T
XM_011510894.1:c.2479-372C>T	XP_011509196.1:n.2479-372C>T
XM_011510891.2:c.2479-372C>T	XP_011509193.1:n.2479-372C>T
XM_011510894.2:c.2479-372C>T	XP_011509196.1:n.2479-372C>T
NM_014521.3:c.2479-372C>T MANE Select	NP_055336.1:n.2479-372C>T
NM_001371302.1:c.2479-372C>T	NP_001358231.1:n.2479-372C>T
NM_001371303.1:c.2479-372C>T	NP_001358232.1:n.2479-372C>T
NM_001371304.1:c.2479-372C>T	NP_001358233.1:n.2479-372C>T
NM_001371305.1:c.2479-372C>T	NP_001358234.1:n.2479-372C>T
NM_001371306.1:c.2479-372C>T	NP_001358235.1:n.2479-372C>T