Canonical Allele Identifier: CA767779885
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1381876825
MyVariant Identifiers: chr2:g.31793425A>G (hg19) chr2:g.31568355A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31568355A>G , CM000664.2:g.31568355A>G GRCh38
NC_000002.11:g.31793425A>G , CM000664.1:g.31793425A>G GRCh37
NC_000002.10:g.31646929A>G NCBI36
NG_008365.1:g.17617T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.281+12265T>C MANE Select ENSP00000477587.1:n.281+12265T>C
ENST00000622030.1:c.281+12265T>C ENSP00000477587.1:n.281+12265T>C
NM_000348.3:c.281+12265T>C NP_000339.2:n.281+12265T>C
XM_011533068.1:c.281+12265T>C XP_011531370.1:n.281+12265T>C
XM_011533070.1:c.27-34589T>C XP_011531372.1:n.27-34589T>C
XM_011533071.1:c.27-34589T>C XP_011531373.1:n.27-34589T>C
XM_011533072.1:c.27-34589T>C XP_011531374.1:n.27-34589T>C
XM_011533072.2:c.27-34589T>C XP_011531374.1:n.27-34589T>C
NM_000348.4:c.281+12265T>C MANE Select NP_000339.2:n.281+12265T>C
Search 100 bp 5'
Search 100 bp 3'