Canonical Allele Identifier: CA892849286
Gene: ALMS1 HGNC NCBI

Linked Data

dbSNP Id: rs1293331923

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73610871A>C , CM000664.2:g.73610871A>C GRCh38
NC_000002.11:g.73837998A>C , CM000664.1:g.73837998A>C GRCh37
NC_000002.10:g.73691506A>C NCBI36
NG_011690.1:g.230119A>C , LRG_741:g.230119A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651434.1:c.3933+1189A>C