Canonical Allele Identifier: CA1619392875
Gene: CYP21A1P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32007071A= , CM000668.2:g.32007071A= GRCh38
NC_000006.11:g.31974848A= , CM000668.1:g.31974848A= GRCh37
NC_000006.10:g.32082826A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342991.10:n.1140A=
ENST00000354927.4:n.702A=
ENST00000623068.1:c.34T= ENSP00000485579.1:p.Leu12=
NR_040090.1:n.1140A=