Canonical Allele Identifier: CA2260368379
Gene: HCRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184456C= , CM000679.2:g.42184456C= GRCh38
NC_000017.10:g.40336474C= , CM000679.1:g.40336474C= GRCh37
NC_000017.9:g.37590000C= NCBI36
NG_011448.1:g.5997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.94G= MANE Select ENSP00000293330.1:p.Ala32=
NM_001524.1:c.94G= MANE Select NP_001515.1:p.Ala32=
Search 100 bp 5'
Search 100 bp 3'