Canonical Allele Identifier: CA2216821958

Gene: HSD3B7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986507A= , CM000678.2:g.30986507A=	GRCh38
NC_000016.9:g.30997828A= , CM000678.1:g.30997828A=	GRCh37
NC_000016.8:g.30905329A=	NCBI36
NG_012346.1:g.6310A=
NG_052948.1:g.34214A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.407A= MANE Select	ENSP00000297679.5:p.Asn136=
ENST00000262520.10:c.407A=	ENSP00000262520.6:p.Asn136=
ENST00000297679.9:c.407A=	ENSP00000297679.5:p.Asn136=
ENST00000562932.5:c.530A=	ENSP00000459852.1:p.Asn177=
ENST00000574447.1:c.407A=	ENSP00000459689.1:p.Asn136=
NM_001142777.1:c.407A=	NP_001136249.1:p.Asn136=
NM_001142778.1:c.407A=	NP_001136250.1:p.Asn136=
NM_025193.3:c.407A=	NP_079469.2:p.Asn136=
XM_005255601.3:c.407A=	XP_005255658.2:p.Asn136=
XM_011545960.1:c.407A=	XP_011544262.1:p.Asn136=
XM_011545961.1:c.407A=	XP_011544263.1:p.Asn136=
XM_011545962.1:c.407A=	XP_011544264.1:p.Asn136=
XM_011545960.2:c.407A=	XP_011544262.1:p.Asn136=
XM_011545962.2:c.407A=	XP_011544264.1:p.Asn136=
XM_017023732.1:c.407A=	XP_016879221.1:p.Asn136=
NM_025193.4:c.407A= MANE Select	NP_079469.2:p.Asn136=
NM_001142777.2:c.407A=	NP_001136249.1:p.Asn136=
NM_001142778.2:c.407A=	NP_001136250.1:p.Asn136=