Canonical Allele Identifier: CA404764796

Gene: B3GNT3

Linked Data

• dbSNP Id: rs36686
• MyVariant Identifiers: chr19:g.17922795G>C (hg19) ; chr19:g.17811986G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17811986G>C , CM000681.2:g.17811986G>C	GRCh38
NC_000019.9:g.17922795G>C , CM000681.1:g.17922795G>C	GRCh37
NC_000019.8:g.17783795G>C	NCBI36
NG_028981.1:g.21877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318683.7:c.983G>C MANE Select	ENSP00000321874.5:p.Arg328Pro
ENST00000318683.6:c.983G>C	ENSP00000321874.5:p.Arg328Pro
ENST00000595387.1:c.983G>C	ENSP00000472638.1:p.Arg328Pro
NM_014256.3:c.983G>C	NP_055071.2:p.Arg328Pro
XM_011527626.1:c.983G>C	XP_011525928.1:p.Arg328Pro
XM_011527627.1:c.983G>C	XP_011525929.1:p.Arg328Pro
XM_011527626.2:c.983G>C	XP_011525928.1:p.Arg328Pro
NM_014256.4:c.983G>C MANE Select	NP_055071.2:p.Arg328Pro