Canonical Allele Identifier: CA346597968
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529371G>C , CM000664.2:g.31529371G>C GRCh38
NC_000002.11:g.31754441G>C , CM000664.1:g.31754441G>C GRCh37
NC_000002.10:g.31607945G>C NCBI36
NG_008365.1:g.56601C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.634C>G MANE Select ENSP00000477587.1:p.Pro212Ala
ENST00000622030.1:c.634C>G ENSP00000477587.1:p.Pro212Ala
NM_000348.3:c.634C>G NP_000339.2:p.Pro212Ala
XM_011533069.1:c.412C>G XP_011531371.1:p.Pro138Ala
XM_011533070.1:c.379C>G XP_011531372.1:p.Pro127Ala
XM_011533071.1:c.379C>G XP_011531373.1:p.Pro127Ala
XM_011533072.1:c.379C>G XP_011531374.1:p.Pro127Ala
XM_011533069.2:c.412C>G XP_011531371.1:p.Pro138Ala
XM_011533072.2:c.379C>G XP_011531374.1:p.Pro127Ala
NM_000348.4:c.634C>G MANE Select NP_000339.2:p.Pro212Ala