Canonical Allele Identifier: CA804009421
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs1326889709

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655313A>G , CM000667.2:g.132655313A>G GRCh38
NC_000005.9:g.131991005A>G , CM000667.1:g.131991005A>G GRCh37
NC_000005.8:g.132018904A>G NCBI36
NG_012090.1:g.2141A>G

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+738T>C
NR_132126.1:n.174+406T>C