Canonical Allele Identifier: CA387720836

Gene: B3GLCT

Linked Data

• gnomAD v4: 13-31269257-A-G
• MyVariant Identifiers: chr13:g.31843394A>G (hg19) ; chr13:g.31269257A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31269257A>G , CM000675.2:g.31269257A>G	GRCh38
NC_000013.10:g.31843394A>G , CM000675.1:g.31843394A>G	GRCh37
NC_000013.9:g.30741394A>G	NCBI36
NG_011732.1:g.74283A>G
NG_011732.2:g.74283A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.640A>G MANE Select	ENSP00000343002.4:p.Thr214Ala
ENST00000343307.4:c.640A>G	ENSP00000343002.4:p.Thr214Ala
ENST00000461652.2:n.255A>G
NM_194318.3:c.640A>G	NP_919299.3:p.Thr214Ala
XM_006719768.2:c.583A>G	XP_006719831.1:p.Thr195Ala
XM_011534936.1:c.640A>G	XP_011533238.1:p.Thr214Ala
XM_011534937.1:c.640A>G	XP_011533239.1:p.Thr214Ala
XM_011534938.1:c.493A>G	XP_011533240.1:p.Thr165Ala
XR_941500.1:n.739A>G
XR_941501.1:n.739A>G
XM_006719768.3:c.583A>G	XP_006719831.1:p.Thr195Ala
XM_011534938.2:c.493A>G	XP_011533240.1:p.Thr165Ala
XM_017020395.1:c.493A>G	XP_016875884.1:p.Thr165Ala
NM_194318.4:c.640A>G MANE Select	NP_919299.3:p.Thr214Ala