Canonical Allele Identifier: CA301006649
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs576838429
MyVariant Identifiers: chr18:g.57026485C>A (hg19) chr18:g.59359253C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359253C>A , CM000680.2:g.59359253C>A GRCh38
NC_000018.9:g.57026485C>A , CM000680.1:g.57026485C>A GRCh37
NC_000018.8:g.55177465C>A NCBI36
NG_012097.1:g.5024G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-9G>T MANE Select ENSP00000251047.4:n.-9G>T
ENST00000251047.5:c.-9G>T ENSP00000251047.4:n.-9G>T
ENST00000587561.1:n.13G>T
NM_005570.3:c.-9G>T NP_005561.1:n.-9G>T
NM_005570.4:c.-9G>T MANE Select NP_005561.1:n.-9G>T
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Search 100 bp 3'