Canonical Allele Identifier: CA3732742

Gene: CYP21A2

Linked Data

• dbSNP Id: rs754606900
• ExAC: 6:32008898 G / T
• gnomAD v2: 6-32008898-G-T
• gnomAD v4: 6-32041121-G-T
• MyVariant Identifiers: chr6:g.32008898G>T (hg19) ; chr6:g.32041121G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041121G>T , CM000668.2:g.32041121G>T	GRCh38
NC_000006.11:g.32008898G>T , CM000668.1:g.32008898G>T	GRCh37
NC_000006.10:g.32116877G>T	NCBI36
NG_007941.2:g.7814G>T
NG_008337.2:g.73254C>A
NG_007941.3:g.7817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1475G>T MANE Select	ENSP00000496625.1:p.Gly492Val
ENST00000418967.6:c.1475G>T	ENSP00000408860.2:p.Gly492Val
ENST00000435122.3:c.1385G>T	ENSP00000415043.2:p.Gly462Val
ENST00000479074.5:n.1616G>T
ENST00000479730.5:n.1591G>T
ENST00000483041.5:n.1644G>T
ENST00000486063.5:n.1454G>T
NM_000500.7:c.1475G>T	NP_000491.4:p.Gly492Val
NM_001128590.3:c.1385G>T	NP_001122062.3:p.Gly462Val
XM_011514314.1:c.1070G>T	XP_011512616.1:p.Gly357Val
NM_000500.9:c.1475G>T MANE Select	NP_000491.4:p.Gly492Val
NM_001368143.1:c.1070G>T	NP_001355072.1:p.Gly357Val
NM_001368144.1:c.1070G>T	NP_001355073.1:p.Gly357Val
NM_001128590.4:c.1385G>T	NP_001122062.3:p.Gly462Val
NM_001368143.2:c.1070G>T	NP_001355072.1:p.Gly357Val
NM_001368144.2:c.1070G>T	NP_001355073.1:p.Gly357Val