Canonical Allele Identifier: CA72698731
Community Standard Title: NC_000003.12:g.33113977G>C
Gene: CRTAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33113977G>C , CM000665.2:g.33113977G>C GRCh38
NC_000003.11:g.33155469G>C , CM000665.1:g.33155469G>C GRCh37
NC_000003.10:g.33130473G>C NCBI36
NG_008122.1:g.5020G>C , LRG_4:g.5020G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006371.4:c.-101G>C , LRG_4t1:c.-101G>C NP_006362.1:n.-101G>C