Canonical Allele Identifier: CA564775668
Gene: SMIM23 HGNC NCBI

Linked Data

dbSNP Id: rs1161509164
gnomAD v2: 5-171203351-G-A
gnomAD v3: 5-171776347-G-A
gnomAD v4: 5-171776347-G-A
MyVariant Identifiers: chr5:g.171203351G>A (hg19) chr5:g.171776347G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.171776347G>A , CM000667.2:g.171776347G>A GRCh38
NC_000005.9:g.171203351G>A , CM000667.1:g.171203351G>A GRCh37
NC_000005.8:g.171135956G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011534623.1:c.3+2389G>A XP_011532925.1:n.3+2389G>A
XM_011534624.1:c.3+2389G>A XP_011532926.1:n.3+2389G>A
XM_011534623.2:c.3+2389G>A XP_011532925.1:n.3+2389G>A
XM_011534624.2:c.3+2389G>A XP_011532926.1:n.3+2389G>A
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