Canonical Allele Identifier: CA10608874

Gene: LAMC2

Linked Data

• ClinVar Variation Id: 293974
• ClinVar RCV Id: RCV000366040
• dbSNP Id: rs574261946
• gnomAD v3: 1-183186091-T-C
• gnomAD v4: 1-183186091-T-C
• MyVariant Identifiers: chr1:g.183155226T>C (hg19) ; chr1:g.183186091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183186091T>C , CM000663.2:g.183186091T>C	GRCh38
NC_000001.10:g.183155226T>C , CM000663.1:g.183155226T>C	GRCh37
NC_000001.9:g.181421849T>C	NCBI36
NG_007079.2:g.4828T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005562.2:c.-262T>C	NP_005553.2:n.-262T>C
NM_018891.2:c.-262T>C	NP_061486.2:n.-262T>C