Canonical Allele Identifier: CA2637931099
Gene: HCRT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184631C>A , CM000679.2:g.42184631C>A GRCh38
NC_000017.10:g.40336649C>A , CM000679.1:g.40336649C>A GRCh37
NC_000017.9:g.37590175C>A NCBI36
NG_011448.1:g.5822G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-103G>T MANE Select ENSP00000293330.1:n.22-103G>T
NM_001524.1:c.22-103G>T MANE Select NP_001515.1:n.22-103G>T