Canonical Allele Identifier: CA519538328
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548777T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680736T>C , CM000686.2:g.7680736T>C GRCh38
NC_000024.9:g.7548777T>C , CM000686.1:g.7548777T>C GRCh37
NC_000024.8:g.7608777T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439805.1:n.488T>C
Search 100 bp 5'
Search 100 bp 3'