Canonical Allele Identifier: CA2260368416
Gene: HCRT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184507G= , CM000679.2:g.42184507G= GRCh38
NC_000017.10:g.40336525G= , CM000679.1:g.40336525G= GRCh37
NC_000017.9:g.37590051G= NCBI36
NG_011448.1:g.5946C=

Transcript Alleles

HGVS Amino-acid change
ENST00000293330.1:c.43C= MANE Select ENSP00000293330.1:p.Leu15=
NM_001524.1:c.43C= MANE Select NP_001515.1:p.Leu15=
Search 100 bp 5'
Search 100 bp 3'