Canonical Allele Identifier: CA404247297

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12768885G>A (hg19) ; chr19:g.12658071G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658071G>A , CM000681.2:g.12658071G>A	GRCh38
NC_000019.9:g.12768885G>A , CM000681.1:g.12768885G>A	GRCh37
NC_000019.8:g.12629885G>A	NCBI36
NG_008318.1:g.13707C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1301C>T MANE Select	ENSP00000395473.2:p.Ala434Val
ENST00000221363.8:c.1298C>T	ENSP00000221363.4:p.Ala433Val
ENST00000456935.6:c.1301C>T	ENSP00000395473.2:p.Ala434Val
ENST00000465830.1:n.465C>T
ENST00000466794.5:n.1200C>T
ENST00000495617.1:n.281-311C>T
NM_000528.3:c.1301C>T	NP_000519.2:p.Ala434Val
NM_001173498.1:c.1298C>T	NP_001166969.1:p.Ala433Val
XM_005259913.1:c.1304C>T	XP_005259970.1:p.Ala435Val
XM_011528017.1:c.200C>T	XP_011526319.1:p.Ala67Val
XM_005259913.2:c.1304C>T	XP_005259970.1:p.Ala435Val
XM_024451518.1:c.200C>T	XP_024307286.1:p.Ala67Val
NM_000528.4:c.1301C>T MANE Select	NP_000519.2:p.Ala434Val
NM_001173498.2:c.1298C>T	NP_001166969.1:p.Ala433Val