Canonical Allele Identifier: CA321167245
Gene: CRYAA HGNC NCBI

Linked Data

dbSNP Id: rs530500347
gnomAD v3: 21-43169037-C-G
gnomAD v4: 21-43169037-C-G
MyVariant Identifiers: chr21:g.43169037C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169037C>G , CM000683.2:g.43169037C>G GRCh38
NG_009823.1:g.5007C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.-63C>G MANE Select ENSP00000291554.2:n.-63C>G
NM_000394.3:c.-63C>G NP_000385.1:n.-63C>G
XR_001755073.1:n.647+2000G>C
NM_000394.4:c.-63C>G MANE Select NP_000385.1:n.-63C>G
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