Canonical Allele Identifier: CA504061411
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026393G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359161G>C , CM000680.2:g.59359161G>C GRCh38
NC_000018.9:g.57026393G>C , CM000680.1:g.57026393G>C GRCh37
NC_000018.8:g.55177373G>C NCBI36
NG_012097.1:g.5116C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251047.6:c.84C>G MANE Select ENSP00000251047.4:p.Val28=
ENST00000251047.5:c.84C>G ENSP00000251047.4:p.Val28=
ENST00000587561.1:n.105C>G
NM_005570.3:c.84C>G NP_005561.1:p.Val28=
NM_005570.4:c.84C>G MANE Select NP_005561.1:p.Val28=