Canonical Allele Identifier: CA343675560
Gene: LAMC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183096538A>C (hg19) chr1:g.183127403A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183127403A>C , CM000663.2:g.183127403A>C GRCh38
NC_000001.10:g.183096538A>C , CM000663.1:g.183096538A>C GRCh37
NC_000001.9:g.181363161A>C NCBI36
NG_011463.1:g.108944A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258341.5:c.3122A>C MANE Select ENSP00000258341.3:p.Lys1041Thr
ENST00000258341.4:c.3122A>C ENSP00000258341.3:p.Lys1041Thr
ENST00000466964.1:n.684A>C
NM_002293.3:c.3122A>C NP_002284.3:p.Lys1041Thr
NM_002293.4:c.3122A>C MANE Select NP_002284.3:p.Lys1041Thr
Search 100 bp 5'
Search 100 bp 3'