Canonical Allele Identifier: CA15551082

Gene: SNTB1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.120598198G>A , CM000670.2:g.120598198G>A	GRCh38
NC_000008.10:g.121610438G>A , CM000670.1:g.121610438G>A	GRCh37
NC_000008.9:g.121679619G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021021.4:c.997-22973C>T MANE Select	NP_066301.1:n.997-22973C>T
ENST00000517992.2:c.997-22973C>T MANE Select	ENSP00000431124.1:n.997-22973C>T
NM_021021.3:c.997-22973C>T	NP_066301.1:n.997-22973C>T
ENST00000395601.7:c.997-22973C>T	ENSP00000378965.3:n.997-22973C>T
ENST00000517992.1:c.997-22973C>T	ENSP00000431124.1:n.997-22973C>T
ENST00000519177.5:n.717-22973C>T
ENST00000648490.1:c.997-22973C>T	ENSP00000497707.1:n.997-22973C>T
XM_011517239.1:c.997-22973C>T	XP_011515541.1:n.997-22973C>T
XM_011517239.2:c.997-22973C>T	XP_011515541.1:n.997-22973C>T