Canonical Allele Identifier: CA8980114
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs765835101

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359249G>C , CM000680.2:g.59359249G>C GRCh38
NC_000018.9:g.57026481G>C , CM000680.1:g.57026481G>C GRCh37
NC_000018.8:g.55177461G>C NCBI36
NG_012097.1:g.5028C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-5C>G MANE Select ENSP00000251047.4:n.-5C>G
ENST00000251047.5:c.-5C>G ENSP00000251047.4:n.-5C>G
ENST00000587561.1:n.17C>G
NM_005570.3:c.-5C>G NP_005561.1:n.-5C>G
NM_005570.4:c.-5C>G MANE Select NP_005561.1:n.-5C>G