Canonical Allele Identifier: CA1583260705
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs556303173

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655338T>G , CM000667.2:g.132655338T>G GRCh38
NC_000005.9:g.131991030T>G , CM000667.1:g.131991030T>G GRCh37
NC_000005.8:g.132018929T>G NCBI36
NG_012090.1:g.2166T>G

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+713A>C
NR_132126.1:n.174+381A>C