Canonical Allele Identifier: CA363505414

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007597G>C (hg19) ; chr6:g.32039820G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039820G>C , CM000668.2:g.32039820G>C	GRCh38
NC_000006.11:g.32007597G>C , CM000668.1:g.32007597G>C	GRCh37
NC_000006.10:g.32115576G>C	NCBI36
NG_007941.2:g.6513G>C
NG_008337.2:g.74555C>G
NG_007941.3:g.6516G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.723G>C MANE Select	ENSP00000496625.1:p.Gln241His
ENST00000418967.6:c.723G>C	ENSP00000408860.2:p.Gln241His
ENST00000435122.3:c.633G>C	ENSP00000415043.2:p.Gln211His
ENST00000462278.1:n.412G>C
ENST00000466779.5:c.*415G>C	ENSP00000417321.1:n.*415G>C
ENST00000466879.5:n.774G>C
ENST00000479074.5:n.781G>C
ENST00000479730.5:n.839G>C
ENST00000483041.5:n.892G>C
ENST00000486063.5:n.903G>C
NM_000500.7:c.723G>C	NP_000491.4:p.Gln241His
NM_001128590.3:c.633G>C	NP_001122062.3:p.Gln211His
XM_011514314.1:c.318G>C	XP_011512616.1:p.Gln106His
NM_000500.9:c.723G>C MANE Select	NP_000491.4:p.Gln241His
NM_001368143.1:c.318G>C	NP_001355072.1:p.Gln106His
NM_001368144.1:c.318G>C	NP_001355073.1:p.Gln106His
NM_001128590.4:c.633G>C	NP_001122062.3:p.Gln211His
NM_001368143.2:c.318G>C	NP_001355072.1:p.Gln106His
NM_001368144.2:c.318G>C	NP_001355073.1:p.Gln106His