Canonical Allele Identifier: CA1815240376

Gene: SNTB1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.120623156C>T , CM000670.2:g.120623156C>T	GRCh38
NC_000008.10:g.121635396C>T , CM000670.1:g.121635396C>T	GRCh37
NC_000008.9:g.121704577C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517992.2:c.996+9288G>A MANE Select	ENSP00000431124.1:n.996+9288G>A
ENST00000648490.1:c.996+9288G>A	ENSP00000497707.1:n.996+9288G>A
ENST00000395601.7:c.996+9288G>A	ENSP00000378965.3:n.996+9288G>A
ENST00000517992.1:c.996+9288G>A	ENSP00000431124.1:n.996+9288G>A
ENST00000519177.5:n.716+9288G>A
NM_021021.3:c.996+9288G>A	NP_066301.1:n.996+9288G>A
XM_011517239.1:c.996+9288G>A	XP_011515541.1:n.996+9288G>A
XM_011517239.2:c.996+9288G>A	XP_011515541.1:n.996+9288G>A
NM_021021.4:c.996+9288G>A MANE Select	NP_066301.1:n.996+9288G>A