Canonical Allele Identifier: CA504061395
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026375T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359143T>G , CM000680.2:g.59359143T>G GRCh38
NC_000018.9:g.57026375T>G , CM000680.1:g.57026375T>G GRCh37
NC_000018.8:g.55177355T>G NCBI36
NG_012097.1:g.5134A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.102A>C MANE Select ENSP00000251047.4:p.Gly34=
ENST00000251047.5:c.102A>C ENSP00000251047.4:p.Gly34=
ENST00000587561.1:n.123A>C
NM_005570.3:c.102A>C NP_005561.1:p.Gly34=
NM_005570.4:c.102A>C MANE Select NP_005561.1:p.Gly34=