Canonical Allele Identifier: CA1694122002
Gene: MTCYBP42 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22748655A= , CM000669.2:g.22748655A= GRCh38
NC_000007.13:g.22788274A= , CM000669.1:g.22788274A= GRCh37
NC_000007.12:g.22754799A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000444653.1:n.150T=