Canonical Allele Identifier: CA337768691
Gene:

Linked Data

dbSNP Id: rs112258157
MyVariant Identifiers: chrY:g.17442372C>G (hg19) chrY:g.15330492C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15330492C>G , CM000686.2:g.15330492C>G GRCh38
NC_000024.9:g.17442372C>G , CM000686.1:g.17442372C>G GRCh37
NC_000024.8:g.15951766C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001756089.1:n.309+18177G>C
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