Canonical Allele Identifier: CA504061394
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1330420690
gnomAD v2: 18-57026375-T-C
MyVariant Identifiers: chr18:g.57026375T>C (hg19) chr18:g.59359143T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.102A>G MANE Select ENSP00000251047.4:p.Gly34=
ENST00000251047.5:c.102A>G ENSP00000251047.4:p.Gly34=
ENST00000587561.1:n.123A>G
NM_005570.3:c.102A>G NP_005561.1:p.Gly34=
NM_005570.4:c.102A>G MANE Select NP_005561.1:p.Gly34=
Search 100 bp 5'
Search 100 bp 3'