Canonical Allele Identifier: CA767792796
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs612224
MyVariant Identifiers: chr2:g.31811870C>T (hg19) chr2:g.31586801C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31586801C>T , CM000664.2:g.31586801C>T GRCh38
NC_000002.11:g.31811870C>T , CM000664.1:g.31811870C>T GRCh37
NC_000002.10:g.31665374C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011533070.1:c.27-53035G>A XP_011531372.1:n.27-53035G>A
XM_011533071.1:c.27-53035G>A XP_011531373.1:n.27-53035G>A
XM_011533072.1:c.27-53035G>A XP_011531374.1:n.27-53035G>A
XM_011533072.2:c.27-53035G>A XP_011531374.1:n.27-53035G>A
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