Canonical Allele Identifier: CA2670662182
Gene: SRD5A3 HGNC NCBI

Linked Data

gnomAD v4: 4-55346255-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346255T>G , CM000666.2:g.55346255T>G GRCh38
NC_000004.11:g.56212422T>G , CM000666.1:g.56212422T>G GRCh37
NC_000004.10:g.55907179T>G NCBI36
NG_028230.1:g.5035T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.9:c.-82T>G MANE Select ENSP00000264228.4:n.-82T>G
ENST00000679707.1:c.-82T>G ENSP00000505713.1:n.-82T>G
ENST00000679836.1:c.-82T>G ENSP00000506601.1:n.-82T>G
ENST00000264228.8:c.-82T>G ENSP00000264228.4:n.-82T>G
NM_024592.4:c.-82T>G NP_078868.1:n.-82T>G
XM_005265766.2:c.-82T>G XP_005265823.1:n.-82T>G
XM_005265767.2:c.-82T>G XP_005265824.1:n.-82T>G
XM_005265766.4:c.-82T>G XP_005265823.1:n.-82T>G
XM_005265767.3:c.-82T>G XP_005265824.1:n.-82T>G
NM_024592.5:c.-82T>G MANE Select NP_078868.1:n.-82T>G