Canonical Allele Identifier: CA363504596

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007535A>C (hg19) ; chr6:g.32039758A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039758A>C , CM000668.2:g.32039758A>C	GRCh38
NC_000006.11:g.32007535A>C , CM000668.1:g.32007535A>C	GRCh37
NC_000006.10:g.32115514A>C	NCBI36
NG_007941.2:g.6451A>C
NG_008337.2:g.74617T>G
NG_007941.3:g.6454A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.661A>C MANE Select	ENSP00000496625.1:p.Asn221His
ENST00000418967.6:c.661A>C	ENSP00000408860.2:p.Asn221His
ENST00000435122.3:c.571A>C	ENSP00000415043.2:p.Asn191His
ENST00000462278.1:n.350A>C
ENST00000466779.5:c.*353A>C	ENSP00000417321.1:n.*353A>C
ENST00000466879.5:n.712A>C
ENST00000479074.5:n.719A>C
ENST00000479730.5:n.777A>C
ENST00000483041.5:n.830A>C
ENST00000486063.5:n.841A>C
NM_000500.7:c.661A>C	NP_000491.4:p.Asn221His
NM_001128590.3:c.571A>C	NP_001122062.3:p.Asn191His
XM_011514314.1:c.256A>C	XP_011512616.1:p.Asn86His
NM_000500.9:c.661A>C MANE Select	NP_000491.4:p.Asn221His
NM_001368143.1:c.256A>C	NP_001355072.1:p.Asn86His
NM_001368144.1:c.256A>C	NP_001355073.1:p.Asn86His
NM_001128590.4:c.571A>C	NP_001122062.3:p.Asn191His
NM_001368143.2:c.256A>C	NP_001355072.1:p.Asn86His
NM_001368144.2:c.256A>C	NP_001355073.1:p.Asn86His