Canonical Allele Identifier: CA8018043
Gene: HSD3B7 HGNC NCBI

Linked Data

dbSNP Id: rs550398099

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986879C>G , CM000678.2:g.30986879C>G GRCh38
NC_000016.9:g.30998200C>G , CM000678.1:g.30998200C>G GRCh37
NC_000016.8:g.30905701C>G NCBI36
NG_012346.1:g.6682C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297679.10:c.571C>G MANE Select ENSP00000297679.5:p.Pro191Ala
ENST00000262520.10:c.531+175C>G ENSP00000262520.6:n.531+175C>G
ENST00000297679.9:c.571C>G ENSP00000297679.5:p.Pro191Ala
NM_001142777.1:c.531+175C>G NP_001136249.1:n.531+175C>G
NM_001142778.1:c.531+175C>G NP_001136250.1:n.531+175C>G
NM_025193.3:c.571C>G NP_079469.2:p.Pro191Ala
XM_005255601.3:c.571C>G XP_005255658.2:p.Pro191Ala
XM_011545960.1:c.571C>G XP_011544262.1:p.Pro191Ala
XM_011545961.1:c.571C>G XP_011544263.1:p.Pro191Ala
XM_011545962.1:c.531+175C>G XP_011544264.1:n.531+175C>G
XM_011545960.2:c.571C>G XP_011544262.1:p.Pro191Ala
XM_011545962.2:c.531+175C>G XP_011544264.1:n.531+175C>G
XM_017023732.1:c.531+175C>G XP_016879221.1:n.531+175C>G
NM_025193.4:c.571C>G MANE Select NP_079469.2:p.Pro191Ala
NM_001142777.2:c.531+175C>G NP_001136249.1:n.531+175C>G
NM_001142778.2:c.531+175C>G NP_001136250.1:n.531+175C>G