Canonical Allele Identifier: CA807545490
Gene: SMIM23 HGNC NCBI

Linked Data

dbSNP Id: rs181019664

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.171776266G>A , CM000667.2:g.171776266G>A GRCh38
NC_000005.9:g.171203270G>A , CM000667.1:g.171203270G>A GRCh37
NC_000005.8:g.171135875G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011534623.1:c.3+2308G>A XP_011532925.1:n.3+2308G>A
XM_011534624.1:c.3+2308G>A XP_011532926.1:n.3+2308G>A
XM_011534623.2:c.3+2308G>A XP_011532925.1:n.3+2308G>A
XM_011534624.2:c.3+2308G>A XP_011532926.1:n.3+2308G>A