Canonical Allele Identifier: CA224916

Gene: SRD5A2

Linked Data

• ClinVar Variation Id: 97411
• ClinVar RCV Id: RCV000083661
• dbSNP Id: rs61748126
• MyVariant Identifiers: chr2:g.31754493G>C (hg19) ; chr2:g.31529423G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529423G>C , CM000664.2:g.31529423G>C	GRCh38
NC_000002.11:g.31754493G>C , CM000664.1:g.31754493G>C	GRCh37
NC_000002.10:g.31607997G>C	NCBI36
NG_008365.1:g.56549C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.582C>G MANE Select	ENSP00000477587.1:p.Phe194Leu
ENST00000622030.1:c.582C>G	ENSP00000477587.1:p.Phe194Leu
NM_000348.3:c.582C>G	NP_000339.2:p.Phe194Leu
XM_011533069.1:c.360C>G	XP_011531371.1:p.Phe120Leu
XM_011533070.1:c.327C>G	XP_011531372.1:p.Phe109Leu
XM_011533071.1:c.327C>G	XP_011531373.1:p.Phe109Leu
XM_011533072.1:c.327C>G	XP_011531374.1:p.Phe109Leu
XM_011533069.2:c.360C>G	XP_011531371.1:p.Phe120Leu
XM_011533072.2:c.327C>G	XP_011531374.1:p.Phe109Leu
NM_000348.4:c.582C>G MANE Select	NP_000339.2:p.Phe194Leu