Canonical Allele Identifier: CA404256175

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776208T>G (hg19) ; chr19:g.12665394T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665394T>G , CM000681.2:g.12665394T>G	GRCh38
NC_000019.9:g.12776208T>G , CM000681.1:g.12776208T>G	GRCh37
NC_000019.8:g.12637208T>G	NCBI36
NG_008318.1:g.6384A>C
NG_015814.1:g.3591T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.394A>C MANE Select	ENSP00000395473.2:p.Thr132Pro
ENST00000221363.8:c.394A>C	ENSP00000221363.4:p.Thr132Pro
ENST00000456935.6:c.394A>C	ENSP00000395473.2:p.Thr132Pro
ENST00000466794.5:n.376A>C
ENST00000486847.2:c.291A>C	ENSP00000470174.1:p.Arg97Ser
ENST00000596512.5:n.332A>C
ENST00000597961.1:c.385A>C	ENSP00000472710.1:p.Thr129Pro
ENST00000598876.1:c.421A>C	ENSP00000470533.1:p.Thr141Pro
ENST00000600281.1:n.435A>C
NM_000528.3:c.394A>C	NP_000519.2:p.Thr132Pro
NM_001173498.1:c.394A>C	NP_001166969.1:p.Thr132Pro
XM_005259913.1:c.394A>C	XP_005259970.1:p.Thr132Pro
XM_005259913.2:c.394A>C	XP_005259970.1:p.Thr132Pro
XM_024451518.1:c.-625A>C	XP_024307286.1:n.-625A>C
NM_000528.4:c.394A>C MANE Select	NP_000519.2:p.Thr132Pro
NM_001173498.2:c.394A>C	NP_001166969.1:p.Thr132Pro