Canonical Allele Identifier: CA410604565
Gene: CRYAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43169262A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169262A>C , CM000683.2:g.43169262A>C GRCh38
NG_009823.1:g.5232A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.163A>C MANE Select ENSP00000291554.2:p.Thr55Pro
ENST00000482775.1:n.176A>C
NM_000394.3:c.163A>C NP_000385.1:p.Thr55Pro
XR_001755073.1:n.647+1775T>G
NM_000394.4:c.163A>C MANE Select NP_000385.1:p.Thr55Pro
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