Canonical Allele Identifier: CA584696374

Gene: SNTB1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.120682410C>G , CM000670.2:g.120682410C>G	GRCh38
NC_000008.10:g.121694650C>G , CM000670.1:g.121694650C>G	GRCh37
NC_000008.9:g.121763831C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517992.2:c.788+11282G>C MANE Select	ENSP00000431124.1:n.788+11282G>C
ENST00000648490.1:c.788+11282G>C	ENSP00000497707.1:n.788+11282G>C
ENST00000395601.7:c.788+11282G>C	ENSP00000378965.3:n.788+11282G>C
ENST00000517992.1:c.788+11282G>C	ENSP00000431124.1:n.788+11282G>C
ENST00000519177.5:n.508+11282G>C
ENST00000519298.1:n.217+11282G>C
NM_021021.3:c.788+11282G>C	NP_066301.1:n.788+11282G>C
XM_011517239.1:c.788+11282G>C	XP_011515541.1:n.788+11282G>C
XM_011517239.2:c.788+11282G>C	XP_011515541.1:n.788+11282G>C
NM_021021.4:c.788+11282G>C MANE Select	NP_066301.1:n.788+11282G>C