Canonical Allele Identifier: CA425627098
Gene: SRD5A2 HGNC NCBI

Linked Data

gnomAD v4: 2-31580676-G-T
MyVariant Identifiers: chr2:g.31805746G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580676G>T , CM000664.2:g.31580676G>T GRCh38
NC_000002.11:g.31805746G>T , CM000664.1:g.31805746G>T GRCh37
NC_000002.10:g.31659250G>T NCBI36
NG_008365.1:g.5296C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.225C>A MANE Select ENSP00000477587.1:p.Leu75=
ENST00000622030.1:c.225C>A ENSP00000477587.1:p.Leu75=
NM_000348.3:c.225C>A NP_000339.2:p.Leu75=
XM_011533068.1:c.225C>A XP_011531370.1:p.Leu75=
XM_011533070.1:c.27-46910C>A XP_011531372.1:n.27-46910C>A
XM_011533071.1:c.27-46910C>A XP_011531373.1:n.27-46910C>A
XM_011533072.1:c.27-46910C>A XP_011531374.1:n.27-46910C>A
XM_011533072.2:c.27-46910C>A XP_011531374.1:n.27-46910C>A
NM_000348.4:c.225C>A MANE Select NP_000339.2:p.Leu75=
Search 100 bp 5'
Search 100 bp 3'