Canonical Allele Identifier: CA2260368491
Gene: HCRT HGNC NCBI

Linked Data

dbSNP Id: rs2079924855

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184627A>G , CM000679.2:g.42184627A>G GRCh38
NC_000017.10:g.40336645A>G , CM000679.1:g.40336645A>G GRCh37
NC_000017.9:g.37590171A>G NCBI36
NG_011448.1:g.5826T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-99T>C MANE Select ENSP00000293330.1:n.22-99T>C
NM_001524.1:c.22-99T>C MANE Select NP_001515.1:n.22-99T>C