Canonical Allele Identifier: CA1211807701
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1022854959

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183201867G>T , CM000663.2:g.183201867G>T GRCh38
NC_000001.10:g.183171002G>T , CM000663.1:g.183171002G>T GRCh37
NC_000001.9:g.181437625G>T NCBI36
NG_007079.2:g.20604G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-6014G>T MANE Select ENSP00000264144.4:n.80-6014G>T
ENST00000264144.4:c.80-6014G>T ENSP00000264144.4:n.80-6014G>T
ENST00000493293.5:c.80-6014G>T ENSP00000432063.1:n.80-6014G>T
NM_005562.2:c.80-6014G>T NP_005553.2:n.80-6014G>T
NM_018891.2:c.80-6014G>T NP_061486.2:n.80-6014G>T
XM_017001273.2:c.80-6014G>T XP_016856762.1:n.80-6014G>T
NM_005562.3:c.80-6014G>T MANE Select NP_005553.2:n.80-6014G>T
NM_018891.3:c.80-6014G>T NP_061486.2:n.80-6014G>T