Canonical Allele Identifier: CA504061396
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026378C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359146C>A , CM000680.2:g.59359146C>A GRCh38
NC_000018.9:g.57026378C>A , CM000680.1:g.57026378C>A GRCh37
NC_000018.8:g.55177358C>A NCBI36
NG_012097.1:g.5131G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.99G>T MANE Select ENSP00000251047.4:p.Val33=
ENST00000251047.5:c.99G>T ENSP00000251047.4:p.Val33=
ENST00000587561.1:n.120G>T
NM_005570.3:c.99G>T NP_005561.1:p.Val33=
NM_005570.4:c.99G>T MANE Select NP_005561.1:p.Val33=
Search 100 bp 5'
Search 100 bp 3'