Canonical Allele Identifier: CA301006607
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1020322950

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359248G>A , CM000680.2:g.59359248G>A GRCh38
NC_000018.9:g.57026480G>A , CM000680.1:g.57026480G>A GRCh37
NC_000018.8:g.55177460G>A NCBI36
NG_012097.1:g.5029C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-4C>T MANE Select ENSP00000251047.4:n.-4C>T
ENST00000251047.5:c.-4C>T ENSP00000251047.4:n.-4C>T
ENST00000587561.1:n.18C>T
NM_005570.3:c.-4C>T NP_005561.1:n.-4C>T
NM_005570.4:c.-4C>T MANE Select NP_005561.1:n.-4C>T