Canonical Allele Identifier: CA337399365
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs905879864
gnomAD v3: Y-19570366-G-A
gnomAD v4: Y-19570366-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570366G>A , CM000686.2:g.19570366G>A GRCh38
NC_000024.9:g.21732252G>A , CM000686.1:g.21732252G>A GRCh37
NC_000024.8:g.20191640G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+2796G>A
ENST00000686905.1:n.133+2884G>A
ENST00000693214.1:n.221+2796G>A
ENST00000445715.6:n.101+2884G>A
ENST00000407724.7:n.170+2884G>A
ENST00000445715.5:n.101+2884G>A
ENST00000447202.2:n.123+2415G>A
ENST00000447520.5:n.101+2884G>A
ENST00000459719.6:n.221+2796G>A
ENST00000538014.2:n.240+907G>A
NR_045128.1:n.125+2884G>A
NR_045129.1:n.125+2884G>A