Canonical Allele Identifier: CA337400735
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs372706460
gnomAD v3: Y-19602615-G-A
gnomAD v4: Y-19602615-G-A
MyVariant Identifiers: chrY:g.21764501G>A (hg19) chrY:g.19602615G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19602615G>A , CM000686.2:g.19602615G>A GRCh38
NC_000024.9:g.21764501G>A , CM000686.1:g.21764501G>A GRCh37
NC_000024.8:g.20223889G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000445715.6:n.1250+304G>A
ENST00000253320.8:n.4821+304G>A
ENST00000445715.5:n.1591+304G>A
ENST00000592697.1:n.586+304G>A
NR_045128.1:n.1274+304G>A
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