Canonical Allele Identifier: CA127247442
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs12188917

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655393T>C , CM000667.2:g.132655393T>C GRCh38
NC_000005.9:g.131991085T>C , CM000667.1:g.131991085T>C GRCh37
NC_000005.8:g.132018984T>C NCBI36
NG_012090.1:g.2221T>C

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+658A>G
NR_132126.1:n.174+326A>G