Canonical Allele Identifier: CA321167893
Gene: CRYAA HGNC NCBI

Linked Data

dbSNP Id: rs540097382
gnomAD v3: 21-43169489-G-C
gnomAD v4: 21-43169489-G-C
MyVariant Identifiers: chr21:g.43169489G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169489G>C , CM000683.2:g.43169489G>C GRCh38
NG_009823.1:g.5459G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.189+201G>C MANE Select ENSP00000291554.2:n.189+201G>C
ENST00000482775.1:n.203-44G>C
NM_000394.3:c.189+201G>C NP_000385.1:n.189+201G>C
XR_001755073.1:n.647+1548C>G
NM_000394.4:c.189+201G>C MANE Select NP_000385.1:n.189+201G>C
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