Canonical Allele Identifier: CA504061413
Gene: LMAN1 HGNC NCBI

Linked Data

gnomAD v4: 18-59359164-G-A
MyVariant Identifiers: chr18:g.57026396G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359164G>A , CM000680.2:g.59359164G>A GRCh38
NC_000018.9:g.57026396G>A , CM000680.1:g.57026396G>A GRCh37
NC_000018.8:g.55177376G>A NCBI36
NG_012097.1:g.5113C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251047.6:c.81C>T MANE Select ENSP00000251047.4:p.Phe27=
ENST00000251047.5:c.81C>T ENSP00000251047.4:p.Phe27=
ENST00000587561.1:n.102C>T
NM_005570.3:c.81C>T NP_005561.1:p.Phe27=
NM_005570.4:c.81C>T MANE Select NP_005561.1:p.Phe27=
Search 100 bp 5'
Search 100 bp 3'