Canonical Allele Identifier: CA395642383

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30999119C>A (hg19) ; chr16:g.30987798C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987798C>A , CM000678.2:g.30987798C>A	GRCh38
NC_000016.9:g.30999119C>A , CM000678.1:g.30999119C>A	GRCh37
NC_000016.8:g.30906620C>A	NCBI36
NG_012346.1:g.7601C>A
NG_041829.1:g.27711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.725C>A MANE Select	ENSP00000297679.5:p.Ala242Asp
ENST00000262520.10:c.562C>A	ENSP00000262520.6:p.Pro188Thr
ENST00000297679.9:c.725C>A	ENSP00000297679.5:p.Ala242Asp
NM_001142777.1:c.562C>A	NP_001136249.1:p.Pro188Thr
NM_001142778.1:c.562C>A	NP_001136250.1:p.Pro188Thr
NM_025193.3:c.725C>A	NP_079469.2:p.Ala242Asp
XM_005255601.3:c.725C>A	XP_005255658.2:p.Ala242Asp
XM_011545960.1:c.725C>A	XP_011544262.1:p.Ala242Asp
XM_011545961.1:c.725C>A	XP_011544263.1:p.Ala242Asp
XM_011545962.1:c.562C>A	XP_011544264.1:p.Pro188Thr
XM_011545960.2:c.725C>A	XP_011544262.1:p.Ala242Asp
XM_011545962.2:c.562C>A	XP_011544264.1:p.Pro188Thr
XM_017023732.1:c.562C>A	XP_016879221.1:p.Pro188Thr
NM_025193.4:c.725C>A MANE Select	NP_079469.2:p.Ala242Asp
NM_001142777.2:c.562C>A	NP_001136249.1:p.Pro188Thr
NM_001142778.2:c.562C>A	NP_001136250.1:p.Pro188Thr