Canonical Allele Identifier: CA395641222

Gene: HSD3B7

Linked Data

• ClinVar Variation Id: 594920
• ClinVar RCV Id: RCV000730322
• dbSNP Id: rs1567371833
• MyVariant Identifiers: chr16:g.30998194C>T (hg19) ; chr16:g.30986873C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986873C>T , CM000678.2:g.30986873C>T	GRCh38
NC_000016.9:g.30998194C>T , CM000678.1:g.30998194C>T	GRCh37
NC_000016.8:g.30905695C>T	NCBI36
NG_012346.1:g.6676C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.565C>T MANE Select	ENSP00000297679.5:p.Leu189Phe
ENST00000262520.10:c.531+169C>T	ENSP00000262520.6:n.531+169C>T
ENST00000297679.9:c.565C>T	ENSP00000297679.5:p.Leu189Phe
NM_001142777.1:c.531+169C>T	NP_001136249.1:n.531+169C>T
NM_001142778.1:c.531+169C>T	NP_001136250.1:n.531+169C>T
NM_025193.3:c.565C>T	NP_079469.2:p.Leu189Phe
XM_005255601.3:c.565C>T	XP_005255658.2:p.Leu189Phe
XM_011545960.1:c.565C>T	XP_011544262.1:p.Leu189Phe
XM_011545961.1:c.565C>T	XP_011544263.1:p.Leu189Phe
XM_011545962.1:c.531+169C>T	XP_011544264.1:n.531+169C>T
XM_011545960.2:c.565C>T	XP_011544262.1:p.Leu189Phe
XM_011545962.2:c.531+169C>T	XP_011544264.1:n.531+169C>T
XM_017023732.1:c.531+169C>T	XP_016879221.1:n.531+169C>T
NM_025193.4:c.565C>T MANE Select	NP_079469.2:p.Leu189Phe
NM_001142777.2:c.531+169C>T	NP_001136249.1:n.531+169C>T
NM_001142778.2:c.531+169C>T	NP_001136250.1:n.531+169C>T