Canonical Allele Identifier: CA1336471996

Gene: SH3BP4

Linked Data

• dbSNP Id: rs1693746873

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.234991538G>C , CM000664.2:g.234991538G>C	GRCh38
NC_000002.11:g.235900182G>C , CM000664.1:g.235900182G>C	GRCh37
NC_000002.10:g.235564921G>C	NCBI36
NG_033930.1:g.44555G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392011.7:c.-206-3765G>C MANE Select	ENSP00000375867.2:n.-206-3765G>C
ENST00000344528.8:c.-122-3765G>C	ENSP00000340237.4:n.-122-3765G>C
ENST00000392011.6:c.-206-3765G>C	ENSP00000375867.2:n.-206-3765G>C
ENST00000409212.5:c.-206-3765G>C	ENSP00000386862.1:n.-206-3765G>C
ENST00000416021.5:c.-133+39368G>C	ENSP00000403251.1:n.-133+39368G>C
ENST00000444916.5:c.-206-3765G>C	ENSP00000387995.1:n.-206-3765G>C
ENST00000446904.5:c.-206-3765G>C	ENSP00000415391.1:n.-206-3765G>C
ENST00000462602.6:n.149-3765G>C
NM_014521.2:c.-206-3765G>C	NP_055336.1:n.-206-3765G>C
XM_011510891.1:c.-206-3765G>C	XP_011509193.1:n.-206-3765G>C
XM_011510892.1:c.-206-3765G>C	XP_011509194.1:n.-206-3765G>C
XM_011510894.1:c.-206-3765G>C	XP_011509196.1:n.-206-3765G>C
XM_011510891.2:c.-206-3765G>C	XP_011509193.1:n.-206-3765G>C
XM_011510894.2:c.-206-3765G>C	XP_011509196.1:n.-206-3765G>C
NM_014521.3:c.-206-3765G>C MANE Select	NP_055336.1:n.-206-3765G>C
NM_001371302.1:c.-206-3765G>C	NP_001358231.1:n.-206-3765G>C
NM_001371303.1:c.-206-3765G>C	NP_001358232.1:n.-206-3765G>C
NM_001371304.1:c.-122-3765G>C	NP_001358233.1:n.-122-3765G>C
NM_001371305.1:c.-206-3765G>C	NP_001358234.1:n.-206-3765G>C