Canonical Allele Identifier: CA804009422
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs1388614235

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655314C>T , CM000667.2:g.132655314C>T GRCh38
NC_000005.9:g.131991006C>T , CM000667.1:g.131991006C>T GRCh37
NC_000005.8:g.132018905C>T NCBI36
NG_012090.1:g.2142C>T

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+737G>A
NR_132126.1:n.174+405G>A