Canonical Allele Identifier: CA605710002
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1174973506
gnomAD v2: 12-65632393-T-G
gnomAD v3: 12-65238613-T-G
gnomAD v4: 12-65238613-T-G
MyVariant Identifiers: chr12:g.65632393T>G (hg19) chr12:g.65238613T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238613T>G , CM000674.2:g.65238613T>G GRCh38
NC_000012.11:g.65632393T>G , CM000674.1:g.65632393T>G GRCh37
NC_000012.10:g.63918660T>G NCBI36
NG_016210.1:g.74043T>G
NG_016210.2:g.74043T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1775+32T>G MANE Select ENSP00000308369.2:n.1775+32T>G
ENST00000308330.2:c.1775+32T>G ENSP00000308369.2:n.1775+32T>G
NM_001167614.1:c.1772+32T>G NP_001161086.1:n.1772+32T>G
NM_014319.4:c.1775+32T>G NP_055134.2:n.1775+32T>G
NM_014319.5:c.1775+32T>G MANE Select NP_055134.2:n.1775+32T>G
NM_001167614.2:c.1772+32T>G NP_001161086.1:n.1772+32T>G
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