Canonical Allele Identifier: CA425559912
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1358628170
MyVariant Identifiers: chr2:g.31748946A>G (hg19) chr2:g.31523876A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31523876A>G , CM000664.2:g.31523876A>G GRCh38
NC_000002.11:g.31748946A>G , CM000664.1:g.31748946A>G GRCh37
NC_000002.10:g.31602450A>G NCBI36
NG_008365.1:g.62096T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.*2320T>C MANE Select ENSP00000477587.1:n.*2320T>C
ENST00000622030.1:c.*2320T>C ENSP00000477587.1:n.*2320T>C
XM_011533069.1:c.*2320T>C XP_011531371.1:n.*2320T>C
XM_011533070.1:c.*2320T>C XP_011531372.1:n.*2320T>C
XM_011533071.1:c.*2320T>C XP_011531373.1:n.*2320T>C
XM_011533072.1:c.*2320T>C XP_011531374.1:n.*2320T>C
XM_011533069.2:c.*2320T>C XP_011531371.1:n.*2320T>C
XM_011533072.2:c.*2320T>C XP_011531374.1:n.*2320T>C
NM_000348.4:c.*2320T>C MANE Select NP_000339.2:n.*2320T>C
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