Canonical Allele Identifier: CA1583260697
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs1751996200

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655322T>G , CM000667.2:g.132655322T>G GRCh38
NC_000005.9:g.131991014T>G , CM000667.1:g.131991014T>G GRCh37
NC_000005.8:g.132018913T>G NCBI36
NG_012090.1:g.2150T>G

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+729A>C
NR_132126.1:n.174+397A>C