Canonical Allele Identifier: CA305478979

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1047922864
• MyVariant Identifiers: chr19:g.12776483G>A (hg19) ; chr19:g.12665669G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665669G>A , CM000681.2:g.12665669G>A	GRCh38
NC_000019.9:g.12776483G>A , CM000681.1:g.12776483G>A	GRCh37
NC_000019.8:g.12637483G>A	NCBI36
NG_008318.1:g.6109C>T
NG_015814.1:g.3866G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.262+34C>T MANE Select	ENSP00000395473.2:n.262+34C>T
ENST00000221363.8:c.262+34C>T	ENSP00000221363.4:n.262+34C>T
ENST00000456935.6:c.262+34C>T	ENSP00000395473.2:n.262+34C>T
ENST00000466794.5:n.244+34C>T
ENST00000486847.2:c.160-144C>T	ENSP00000470174.1:n.160-144C>T
ENST00000596512.5:n.201-144C>T
ENST00000597961.1:c.253+34C>T	ENSP00000472710.1:n.253+34C>T
ENST00000598876.1:c.289+34C>T	ENSP00000470533.1:n.289+34C>T
ENST00000600281.1:n.303+34C>T
NM_000528.3:c.262+34C>T	NP_000519.2:n.262+34C>T
NM_001173498.1:c.262+34C>T	NP_001166969.1:n.262+34C>T
XM_005259913.1:c.262+34C>T	XP_005259970.1:n.262+34C>T
XM_005259913.2:c.262+34C>T	XP_005259970.1:n.262+34C>T
XM_024451518.1:c.-757+34C>T	XP_024307286.1:n.-757+34C>T
NM_000528.4:c.262+34C>T MANE Select	NP_000519.2:n.262+34C>T
NM_001173498.2:c.262+34C>T	NP_001166969.1:n.262+34C>T