Canonical Allele Identifier: CA1242198371
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531508A= , CM000664.2:g.31531508A= GRCh38
NC_000002.11:g.31756578A= , CM000664.1:g.31756578A= GRCh37
NC_000002.10:g.31610082A= NCBI36
NG_008365.1:g.54464T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.446-36T= MANE Select ENSP00000477587.1:n.446-36T=
ENST00000622030.1:c.446-36T= ENSP00000477587.1:n.446-36T=
NM_000348.3:c.446-36T= NP_000339.2:n.446-36T=
XM_011533069.1:c.224-36T= XP_011531371.1:n.224-36T=
XM_011533070.1:c.191-36T= XP_011531372.1:n.191-36T=
XM_011533071.1:c.191-36T= XP_011531373.1:n.191-36T=
XM_011533072.1:c.191-36T= XP_011531374.1:n.191-36T=
XM_011533069.2:c.224-36T= XP_011531371.1:n.224-36T=
XM_011533072.2:c.191-36T= XP_011531374.1:n.191-36T=
NM_000348.4:c.446-36T= MANE Select NP_000339.2:n.446-36T=