Canonical Allele Identifier: CA494921009

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30999258A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987937A>G , CM000678.2:g.30987937A>G	GRCh38
NC_000016.9:g.30999258A>G , CM000678.1:g.30999258A>G	GRCh37
NC_000016.8:g.30906759A>G	NCBI36
NG_012346.1:g.7740A>G
NG_041829.1:g.27572T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.864A>G MANE Select	ENSP00000297679.5:p.Pro288=
ENST00000262520.10:c.*110A>G	ENSP00000262520.6:n.*110A>G
ENST00000297679.9:c.864A>G	ENSP00000297679.5:p.Pro288=
NM_001142777.1:c.*110A>G	NP_001136249.1:n.*110A>G
NM_001142778.1:c.*110A>G	NP_001136250.1:n.*110A>G
NM_025193.3:c.864A>G	NP_079469.2:p.Pro288=
XM_005255601.3:c.864A>G	XP_005255658.2:p.Pro288=
XM_011545960.1:c.864A>G	XP_011544262.1:p.Pro288=
XM_011545961.1:c.864A>G	XP_011544263.1:p.Pro288=
XM_011545960.2:c.864A>G	XP_011544262.1:p.Pro288=
XM_011545962.2:c.*110A>G	XP_011544264.1:n.*110A>G
XM_017023732.1:c.*110A>G	XP_016879221.1:n.*110A>G
NM_025193.4:c.864A>G MANE Select	NP_079469.2:p.Pro288=
NM_001142777.2:c.*110A>G	NP_001136249.1:n.*110A>G
NM_001142778.2:c.*110A>G	NP_001136250.1:n.*110A>G