Canonical Allele Identifier: CA410603922
Gene: CRYAA HGNC NCBI

Linked Data

gnomAD v4: 21-43169103-G-T
MyVariant Identifiers: chr21:g.43169103G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43169103G>T , CM000683.2:g.43169103G>T GRCh38
NG_009823.1:g.5073G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291554.6:c.4G>T MANE Select ENSP00000291554.2:p.Asp2Tyr
ENST00000482775.1:n.17G>T
NM_000394.3:c.4G>T NP_000385.1:p.Asp2Tyr
XR_001755073.1:n.647+1934C>A
NM_000394.4:c.4G>T MANE Select NP_000385.1:p.Asp2Tyr
Search 100 bp 5'
Search 100 bp 3'