Canonical Allele Identifier: CA238909576
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1032010543
gnomAD v2: 12-65582213-T-C
gnomAD v3: 12-65188433-T-C
gnomAD v4: 12-65188433-T-C
MyVariant Identifiers: chr12:g.65582213T>C (hg19) chr12:g.65582213_65582214delinsCG (hg19) chr12:g.65188433T>C (hg38) chr12:g.65188433_65188434delinsCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65188433T>C , CM000674.2:g.65188433T>C GRCh38
NC_000012.11:g.65582213T>C , CM000674.1:g.65582213T>C GRCh37
NC_000012.10:g.63868480T>C NCBI36
NG_016210.1:g.23863T>C
NG_016210.2:g.23863T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1522+17315T>C MANE Select ENSP00000308369.2:n.1522+17315T>C
ENST00000308330.2:c.1522+17315T>C ENSP00000308369.2:n.1522+17315T>C
ENST00000541171.1:n.836+18015T>C
NM_001167614.1:c.1522+17315T>C NP_001161086.1:n.1522+17315T>C
NM_014319.4:c.1522+17315T>C NP_055134.2:n.1522+17315T>C
NM_014319.5:c.1522+17315T>C MANE Select NP_055134.2:n.1522+17315T>C
NM_001167614.2:c.1522+17315T>C NP_001161086.1:n.1522+17315T>C
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