Canonical Allele Identifier: CA404255959

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776185C>G (hg19) ; chr19:g.12665371C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665371C>G , CM000681.2:g.12665371C>G	GRCh38
NC_000019.9:g.12776185C>G , CM000681.1:g.12776185C>G	GRCh37
NC_000019.8:g.12637185C>G	NCBI36
NG_008318.1:g.6407G>C
NG_015814.1:g.3568C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.417G>C MANE Select	ENSP00000395473.2:p.Val139=
ENST00000221363.8:c.417G>C	ENSP00000221363.4:p.Val139=
ENST00000456935.6:c.417G>C	ENSP00000395473.2:p.Val139=
ENST00000466794.5:n.399G>C
ENST00000486847.2:c.314G>C	ENSP00000470174.1:p.Cys105Ser
ENST00000596512.5:n.355G>C
ENST00000597961.1:c.408G>C	ENSP00000472710.1:p.Val136=
ENST00000598876.1:c.444G>C	ENSP00000470533.1:p.Val148=
ENST00000600281.1:n.458G>C
NM_000528.3:c.417G>C	NP_000519.2:p.Val139=
NM_001173498.1:c.417G>C	NP_001166969.1:p.Val139=
XM_005259913.1:c.417G>C	XP_005259970.1:p.Val139=
XM_005259913.2:c.417G>C	XP_005259970.1:p.Val139=
XM_024451518.1:c.-602G>C	XP_024307286.1:n.-602G>C
NM_000528.4:c.417G>C MANE Select	NP_000519.2:p.Val139=
NM_001173498.2:c.417G>C	NP_001166969.1:p.Val139=