Canonical Allele Identifier: CA1815240374

Gene: SNTB1

Genomic Alleles

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

Transcript Alleles

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