Canonical Allele Identifier: CA387818961

Gene: B3GLCT

Linked Data

• MyVariant Identifiers: chr13:g.31891711G>C (hg19) ; chr13:g.31317574G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317574G>C , CM000675.2:g.31317574G>C	GRCh38
NC_000013.10:g.31891711G>C , CM000675.1:g.31891711G>C	GRCh37
NC_000013.9:g.30789711G>C	NCBI36
NG_011732.1:g.122600G>C
NG_011732.2:g.122600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.1073G>C MANE Select	ENSP00000343002.4:p.Arg358Thr
ENST00000343307.4:c.1073G>C	ENSP00000343002.4:p.Arg358Thr
NM_194318.3:c.1073G>C	NP_919299.3:p.Arg358Thr
XM_006719768.2:c.1016G>C	XP_006719831.1:p.Arg339Thr
XM_011534936.1:c.1065-6177G>C	XP_011533238.1:n.1065-6177G>C
XM_011534937.1:c.953G>C	XP_011533239.1:p.Arg318Thr
XM_011534938.1:c.926G>C	XP_011533240.1:p.Arg309Thr
XR_941500.1:n.1258G>C
XR_941501.1:n.1138G>C
XM_006719768.3:c.1016G>C	XP_006719831.1:p.Arg339Thr
XM_011534938.2:c.926G>C	XP_011533240.1:p.Arg309Thr
XM_017020395.1:c.926G>C	XP_016875884.1:p.Arg309Thr
NM_194318.4:c.1073G>C MANE Select	NP_919299.3:p.Arg358Thr