Canonical Allele Identifier: CA363501647

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1776069565
• MyVariant Identifiers: chr6:g.32006986G>A (hg19) ; chr6:g.32039209G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039209G>A , CM000668.2:g.32039209G>A	GRCh38
NC_000006.11:g.32006986G>A , CM000668.1:g.32006986G>A	GRCh37
NC_000006.10:g.32114965G>A	NCBI36
NG_007941.2:g.5902G>A
NG_008337.2:g.75166C>T
NG_007941.3:g.5905G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.408G>A MANE Select	ENSP00000496625.1:p.Met136Ile
ENST00000418967.6:c.408G>A	ENSP00000408860.2:p.Met136Ile
ENST00000435122.3:c.318G>A	ENSP00000415043.2:p.Met106Ile
ENST00000464325.5:n.329G>A
ENST00000466779.5:c.*100G>A	ENSP00000417321.1:n.*100G>A
ENST00000466879.5:n.459G>A
ENST00000469053.5:c.*100G>A	ENSP00000418104.1:n.*100G>A
ENST00000471671.4:c.408G>A	ENSP00000418561.1:p.Met136Ile
ENST00000478281.5:c.441G>A	ENSP00000419572.1:p.Met147Ile
ENST00000479074.5:n.466G>A
ENST00000479730.5:n.563G>A
ENST00000483041.5:n.577G>A
ENST00000486063.5:n.588G>A
ENST00000488465.1:n.416G>A
NM_000500.7:c.408G>A	NP_000491.4:p.Met136Ile
NM_001128590.3:c.318G>A	NP_001122062.3:p.Met106Ile
XM_011514314.1:c.3G>A	XP_011512616.1:p.Met1Ile
NM_000500.9:c.408G>A MANE Select	NP_000491.4:p.Met136Ile
NM_001368143.1:c.3G>A	NP_001355072.1:p.Met1Ile
NM_001368144.1:c.3G>A	NP_001355073.1:p.Met1Ile
NM_001128590.4:c.318G>A	NP_001122062.3:p.Met106Ile
NM_001368143.2:c.3G>A	NP_001355072.1:p.Met1Ile
NM_001368144.2:c.3G>A	NP_001355073.1:p.Met1Ile