Canonical Allele Identifier: CA494920643
Gene: HSD3B7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30997844C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986523C>G , CM000678.2:g.30986523C>G GRCh38
NC_000016.9:g.30997844C>G , CM000678.1:g.30997844C>G GRCh37
NC_000016.8:g.30905345C>G NCBI36
NG_012346.1:g.6326C>G
NG_052948.1:g.34230C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297679.10:c.423C>G MANE Select ENSP00000297679.5:p.Pro141=
ENST00000262520.10:c.423C>G ENSP00000262520.6:p.Pro141=
ENST00000297679.9:c.423C>G ENSP00000297679.5:p.Pro141=
ENST00000562932.5:c.546C>G ENSP00000459852.1:p.Pro182=
ENST00000574447.1:c.423C>G ENSP00000459689.1:p.Pro141=
NM_001142777.1:c.423C>G NP_001136249.1:p.Pro141=
NM_001142778.1:c.423C>G NP_001136250.1:p.Pro141=
NM_025193.3:c.423C>G NP_079469.2:p.Pro141=
XM_005255601.3:c.423C>G XP_005255658.2:p.Pro141=
XM_011545960.1:c.423C>G XP_011544262.1:p.Pro141=
XM_011545961.1:c.423C>G XP_011544263.1:p.Pro141=
XM_011545962.1:c.423C>G XP_011544264.1:p.Pro141=
XM_011545960.2:c.423C>G XP_011544262.1:p.Pro141=
XM_011545962.2:c.423C>G XP_011544264.1:p.Pro141=
XM_017023732.1:c.423C>G XP_016879221.1:p.Pro141=
NM_025193.4:c.423C>G MANE Select NP_079469.2:p.Pro141=
NM_001142777.2:c.423C>G NP_001136249.1:p.Pro141=
NM_001142778.2:c.423C>G NP_001136250.1:p.Pro141=