Canonical Allele Identifier: CA1211824032
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1660079118
gnomAD v4: 1-183239941-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183239941G>T , CM000663.2:g.183239941G>T GRCh38
NC_000001.10:g.183209076G>T , CM000663.1:g.183209076G>T GRCh37
NC_000001.9:g.181475699G>T NCBI36
NG_007079.2:g.58678G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3070-99G>T MANE Select ENSP00000264144.4:n.3070-99G>T
ENST00000264144.4:c.3070-99G>T ENSP00000264144.4:n.3070-99G>T
ENST00000461729.1:n.441G>T
ENST00000493293.5:c.3070-99G>T ENSP00000432063.1:n.3070-99G>T
NM_005562.2:c.3070-99G>T NP_005553.2:n.3070-99G>T
NM_018891.2:c.3070-99G>T NP_061486.2:n.3070-99G>T
NM_005562.3:c.3070-99G>T MANE Select NP_005553.2:n.3070-99G>T
NM_018891.3:c.3070-99G>T NP_061486.2:n.3070-99G>T
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