Canonical Allele Identifier: CA2260368363
Gene: HCRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184414A= , CM000679.2:g.42184414A= GRCh38
NC_000017.10:g.40336432A= , CM000679.1:g.40336432A= GRCh37
NC_000017.9:g.37589958A= NCBI36
NG_011448.1:g.6039T=

Transcript Alleles

HGVS Amino-acid change
ENST00000293330.1:c.136T= MANE Select ENSP00000293330.1:p.Ser46=
NM_001524.1:c.136T= MANE Select NP_001515.1:p.Ser46=
Search 100 bp 5'
Search 100 bp 3'