Canonical Allele Identifier: CA425566456
Gene: SRD5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.31751207G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526137G>C , CM000664.2:g.31526137G>C GRCh38
NC_000002.11:g.31751207G>C , CM000664.1:g.31751207G>C GRCh37
NC_000002.10:g.31604711G>C NCBI36
NG_008365.1:g.59835C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.*59C>G MANE Select ENSP00000477587.1:n.*59C>G
ENST00000622030.1:c.*59C>G ENSP00000477587.1:n.*59C>G
NM_000348.3:c.*59C>G NP_000339.2:n.*59C>G
XM_011533069.1:c.*59C>G XP_011531371.1:n.*59C>G
XM_011533070.1:c.*59C>G XP_011531372.1:n.*59C>G
XM_011533071.1:c.*59C>G XP_011531373.1:n.*59C>G
XM_011533072.1:c.*59C>G XP_011531374.1:n.*59C>G
XM_011533069.2:c.*59C>G XP_011531371.1:n.*59C>G
XM_011533072.2:c.*59C>G XP_011531374.1:n.*59C>G
NM_000348.4:c.*59C>G MANE Select NP_000339.2:n.*59C>G
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