Canonical Allele Identifier: CA2637931110
Gene: HCRT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184637T>C , CM000679.2:g.42184637T>C GRCh38
NC_000017.10:g.40336655T>C , CM000679.1:g.40336655T>C GRCh37
NC_000017.9:g.37590181T>C NCBI36
NG_011448.1:g.5816A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-109A>G MANE Select ENSP00000293330.1:n.22-109A>G
NM_001524.1:c.22-109A>G MANE Select NP_001515.1:n.22-109A>G