Canonical Allele Identifier: CA301006625
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1000422602
gnomAD v2: 18-57026483-T-A
gnomAD v4: 18-59359251-T-A
MyVariant Identifiers: chr18:g.57026483T>A (hg19) chr18:g.59359251T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359251T>A , CM000680.2:g.59359251T>A GRCh38
NC_000018.9:g.57026483T>A , CM000680.1:g.57026483T>A GRCh37
NC_000018.8:g.55177463T>A NCBI36
NG_012097.1:g.5026A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-7A>T MANE Select ENSP00000251047.4:n.-7A>T
ENST00000251047.5:c.-7A>T ENSP00000251047.4:n.-7A>T
ENST00000587561.1:n.15A>T
NM_005570.3:c.-7A>T NP_005561.1:n.-7A>T
NM_005570.4:c.-7A>T MANE Select NP_005561.1:n.-7A>T
Search 100 bp 5'
Search 100 bp 3'