Canonical Allele Identifier: CA1583260707
Gene: TH2LCRR HGNC NCBI

Linked Data

dbSNP Id: rs3091308

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132655340G>T , CM000667.2:g.132655340G>T GRCh38
NC_000005.9:g.131991032G>T , CM000667.1:g.131991032G>T GRCh37
NC_000005.8:g.132018931G>T NCBI36
NG_012090.1:g.2168G>T

Transcript Alleles

HGVS Amino-acid change
NR_132125.1:n.104+711C>A
NR_132126.1:n.174+379C>A