Canonical Allele Identifier: CA2260368509
Gene: HCRT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184668T= , CM000679.2:g.42184668T= GRCh38
NC_000017.10:g.40336686T= , CM000679.1:g.40336686T= GRCh37
NC_000017.9:g.37590212T= NCBI36
NG_011448.1:g.5785A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-140A= MANE Select ENSP00000293330.1:n.22-140A=
NM_001524.1:c.22-140A= MANE Select NP_001515.1:n.22-140A=
Search 100 bp 5'
Search 100 bp 3'