Canonical Allele Identifier: CA6406669

Gene: LTBR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6388415G>T , CM000674.2:g.6388415G>T	GRCh38
NC_000012.11:g.6497581G>T , CM000674.1:g.6497581G>T	GRCh37
NC_000012.10:g.6367842G>T	NCBI36
NG_033039.1:g.18048G>T
NG_033039.2:g.18048G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002342.3:c.685G>T MANE Select	NP_002333.1:p.Ala229Ser
ENST00000228918.9:c.685G>T MANE Select	ENSP00000228918.4:p.Ala229Ser
NM_001270987.1:c.628G>T	NP_001257916.1:p.Ala210Ser
NM_001270987.2:c.628G>T	NP_001257916.1:p.Ala210Ser
NM_002342.2:c.685G>T	NP_002333.1:p.Ala229Ser
ENST00000228918.8:c.685G>T	ENSP00000228918.4:p.Ala229Ser
ENST00000539925.5:c.628G>T	ENSP00000440875.1:p.Ala210Ser
ENST00000541005.1:n.162G>T
ENST00000541102.1:c.347-385G>T	ENSP00000438605.1:n.347-385G>T
ENST00000543190.5:c.*42G>T	ENSP00000438955.1:n.*42G>T
ENST00000543542.1:n.24G>T
ENST00000544454.5:c.*30G>T	ENSP00000437954.1:n.*30G>T
XM_005253688.1:c.668-385G>T	XP_005253745.1:n.668-385G>T
XM_005253688.2:c.668-385G>T	XP_005253745.1:n.668-385G>T
XM_006718983.2:c.*30G>T	XP_006719046.1:n.*30G>T
XM_006718983.3:c.*30G>T	XP_006719046.1:n.*30G>T