Canonical Allele Identifier: CA425627476
Gene: SRD5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.31805824G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580754G>C , CM000664.2:g.31580754G>C GRCh38
NC_000002.11:g.31805824G>C , CM000664.1:g.31805824G>C GRCh37
NC_000002.10:g.31659328G>C NCBI36
NG_008365.1:g.5218C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.147C>G MANE Select ENSP00000477587.1:p.Ala49=
ENST00000622030.1:c.147C>G ENSP00000477587.1:p.Ala49=
NM_000348.3:c.147C>G NP_000339.2:p.Ala49=
XM_011533068.1:c.147C>G XP_011531370.1:p.Ala49=
XM_011533070.1:c.27-46988C>G XP_011531372.1:n.27-46988C>G
XM_011533071.1:c.27-46988C>G XP_011531373.1:n.27-46988C>G
XM_011533072.1:c.27-46988C>G XP_011531374.1:n.27-46988C>G
XM_011533072.2:c.27-46988C>G XP_011531374.1:n.27-46988C>G
NM_000348.4:c.147C>G MANE Select NP_000339.2:p.Ala49=
Search 100 bp 5'
Search 100 bp 3'