Canonical Allele Identifier: CA337532955
Gene:

Linked Data

dbSNP Id: rs202159348 rs2124007683 rs2124007686
MyVariant Identifiers: chrY:g.23476015T>G (hg19) chrY:g.21314129T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.21314129T>G , CM000686.2:g.21314129T>G GRCh38
NC_000024.9:g.23476015T>G , CM000686.1:g.23476015T>G GRCh37
NC_000024.8:g.21885403T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437359.1:n.289-49T>G
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