Canonical Allele Identifier: CA337532922
Gene:

Linked Data

dbSNP Id: rs111918838 rs2124007655 rs2124007661
MyVariant Identifiers: chrY:g.23474348T>A (hg19) chrY:g.21312462T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.21312462T>A , CM000686.2:g.21312462T>A GRCh38
NC_000024.9:g.23474348T>A , CM000686.1:g.23474348T>A GRCh37
NC_000024.8:g.21883736T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437359.1:n.288+462T>A
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