Canonical Allele Identifier: CA1242214663
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1666757858

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567506T>A , CM000664.2:g.31567506T>A GRCh38
NC_000002.11:g.31792576T>A , CM000664.1:g.31792576T>A GRCh37
NC_000002.10:g.31646080T>A NCBI36
NG_008365.1:g.18466A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13114A>T MANE Select ENSP00000477587.1:n.281+13114A>T
ENST00000622030.1:c.281+13114A>T ENSP00000477587.1:n.281+13114A>T
NM_000348.3:c.281+13114A>T NP_000339.2:n.281+13114A>T
XM_011533068.1:c.281+13114A>T XP_011531370.1:n.281+13114A>T
XM_011533070.1:c.27-33740A>T XP_011531372.1:n.27-33740A>T
XM_011533071.1:c.27-33740A>T XP_011531373.1:n.27-33740A>T
XM_011533072.1:c.27-33740A>T XP_011531374.1:n.27-33740A>T
XM_011533072.2:c.27-33740A>T XP_011531374.1:n.27-33740A>T
NM_000348.4:c.281+13114A>T MANE Select NP_000339.2:n.281+13114A>T