Canonical Allele Identifier: CA1261040925
Gene: ALMS1 HGNC NCBI

Linked Data

dbSNP Id: rs1675924259

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73610770A>G , CM000664.2:g.73610770A>G GRCh38
NC_000002.11:g.73837897A>G , CM000664.1:g.73837897A>G GRCh37
NC_000002.10:g.73691405A>G NCBI36
NG_011690.1:g.230018A>G , LRG_741:g.230018A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651434.1:c.3933+1088A>G
ENST00000490821.1:n.555A>G