Canonical Allele Identifier: CA387819191

Gene: B3GLCT

Linked Data

• MyVariant Identifiers: chr13:g.31891822G>T (hg19) ; chr13:g.31317685G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317685G>T , CM000675.2:g.31317685G>T	GRCh38
NC_000013.10:g.31891822G>T , CM000675.1:g.31891822G>T	GRCh37
NC_000013.9:g.30789822G>T	NCBI36
NG_011732.1:g.122711G>T
NG_011732.2:g.122711G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343307.5:c.1184G>T MANE Select	ENSP00000343002.4:p.Gly395Val
ENST00000343307.4:c.1184G>T	ENSP00000343002.4:p.Gly395Val
NM_194318.3:c.1184G>T	NP_919299.3:p.Gly395Val
XM_006719768.2:c.1127G>T	XP_006719831.1:p.Gly376Val
XM_011534936.1:c.1065-6066G>T	XP_011533238.1:n.1065-6066G>T
XM_011534937.1:c.1064G>T	XP_011533239.1:p.Gly355Val
XM_011534938.1:c.1037G>T	XP_011533240.1:p.Gly346Val
XM_006719768.3:c.1127G>T	XP_006719831.1:p.Gly376Val
XM_011534938.2:c.1037G>T	XP_011533240.1:p.Gly346Val
XM_017020395.1:c.1037G>T	XP_016875884.1:p.Gly346Val
NM_194318.4:c.1184G>T MANE Select	NP_919299.3:p.Gly395Val