Canonical Allele Identifier: CA2260368413
Gene: HCRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184504G= , CM000679.2:g.42184504G= GRCh38
NC_000017.10:g.40336522G= , CM000679.1:g.40336522G= GRCh37
NC_000017.9:g.37590048G= NCBI36
NG_011448.1:g.5949C=

Transcript Alleles

HGVS Amino-acid change
ENST00000293330.1:c.46C= MANE Select ENSP00000293330.1:p.Leu16=
NM_001524.1:c.46C= MANE Select NP_001515.1:p.Leu16=
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