Canonical Allele Identifier: CA8980116
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs778898915
ExAC: 18:57026491 C / G
gnomAD v2: 18-57026491-C-G
gnomAD v4: 18-59359259-C-G
MyVariant Identifiers: chr18:g.57026491C>G (hg19) chr18:g.59359259C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359259C>G , CM000680.2:g.59359259C>G GRCh38
NC_000018.9:g.57026491C>G , CM000680.1:g.57026491C>G GRCh37
NC_000018.8:g.55177471C>G NCBI36
NG_012097.1:g.5018G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-15G>C MANE Select ENSP00000251047.4:n.-15G>C
ENST00000251047.5:c.-15G>C ENSP00000251047.4:n.-15G>C
ENST00000587561.1:n.7G>C
NM_005570.3:c.-15G>C NP_005561.1:n.-15G>C
NM_005570.4:c.-15G>C MANE Select NP_005561.1:n.-15G>C
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