Canonical Allele Identifier: CA772085968
Gene: HCRT HGNC NCBI

Linked Data

dbSNP Id: rs1229908214

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42184629G>A , CM000679.2:g.42184629G>A GRCh38
NC_000017.10:g.40336647G>A , CM000679.1:g.40336647G>A GRCh37
NC_000017.9:g.37590173G>A NCBI36
NG_011448.1:g.5824C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293330.1:c.22-101C>T MANE Select ENSP00000293330.1:n.22-101C>T
NM_001524.1:c.22-101C>T MANE Select NP_001515.1:n.22-101C>T