Canonical Allele Identifier: CA337491769
Gene: EIF1AY HGNC NCBI

Linked Data

dbSNP Id: rs780869630
gnomAD v3: Y-20583281-T-A
gnomAD v4: Y-20583281-T-A
MyVariant Identifiers: chrY:g.22745167T>A (hg19) chrY:g.20583281T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20583281T>A , CM000686.2:g.20583281T>A GRCh38
NC_000024.9:g.22745167T>A , CM000686.1:g.22745167T>A GRCh37
NC_000024.8:g.21154555T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361365.7:c.204+588T>A MANE Select ENSP00000354722.2:n.204+588T>A
ENST00000361365.6:c.204+588T>A ENSP00000354722.2:n.204+588T>A
ENST00000382772.3:c.204+588T>A ENSP00000372222.3:n.204+588T>A
ENST00000465253.1:n.298+588T>A
NM_001278612.1:c.204+588T>A NP_001265541.1:n.204+588T>A
NM_004681.3:c.204+588T>A NP_004672.2:n.204+588T>A
NM_004681.4:c.204+588T>A MANE Select NP_004672.2:n.204+588T>A
NM_001278612.2:c.204+588T>A NP_001265541.1:n.204+588T>A
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