Canonical Allele Identifier: CA337399516

Gene: TXLNGY

Linked Data

• dbSNP Id: rs770701128
• gnomAD v3: Y-19574322-C-T
• gnomAD v4: Y-19574322-C-T
• MyVariant Identifiers: chrY:g.21736208C>T (hg19) ; chrY:g.19574322C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19574322C>T , CM000686.2:g.19574322C>T	GRCh38
NC_000024.9:g.21736208C>T , CM000686.1:g.21736208C>T	GRCh37
NC_000024.8:g.20195596C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.199+6752C>T
ENST00000686905.1:n.133+6840C>T
ENST00000693214.1:n.221+6752C>T
ENST00000445715.6:n.101+6840C>T
ENST00000407724.7:n.170+6840C>T
ENST00000445715.5:n.101+6840C>T
ENST00000447202.2:n.123+6371C>T
ENST00000447520.5:n.101+6840C>T
ENST00000459719.6:n.221+6752C>T
ENST00000538014.2:n.240+4863C>T
NR_045128.1:n.125+6840C>T
NR_045129.1:n.125+6840C>T