Canonical Allele Identifier: CA50344406
Gene: ALMS1 HGNC NCBI

Linked Data

dbSNP Id: rs975830561

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73610739G>A , CM000664.2:g.73610739G>A GRCh38
NC_000002.11:g.73837866G>A , CM000664.1:g.73837866G>A GRCh37
NC_000002.10:g.73691374G>A NCBI36
NG_011690.1:g.229987G>A , LRG_741:g.229987G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651434.1:c.3933+1057G>A
ENST00000490821.1:n.524G>A