Canonical Allele Identifier: CA494921034

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30999291T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987970T>C , CM000678.2:g.30987970T>C	GRCh38
NC_000016.9:g.30999291T>C , CM000678.1:g.30999291T>C	GRCh37
NC_000016.8:g.30906792T>C	NCBI36
NG_012346.1:g.7773T>C
NG_041829.1:g.27539A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.897T>C MANE Select	ENSP00000297679.5:p.Ala299=
ENST00000262520.10:c.*143T>C	ENSP00000262520.6:n.*143T>C
ENST00000297679.9:c.897T>C	ENSP00000297679.5:p.Ala299=
NM_001142777.1:c.*143T>C	NP_001136249.1:n.*143T>C
NM_001142778.1:c.*143T>C	NP_001136250.1:n.*143T>C
NM_025193.3:c.897T>C	NP_079469.2:p.Ala299=
XM_005255601.3:c.897T>C	XP_005255658.2:p.Ala299=
XM_011545960.1:c.897T>C	XP_011544262.1:p.Ala299=
XM_011545961.1:c.897T>C	XP_011544263.1:p.Ala299=
XM_011545960.2:c.897T>C	XP_011544262.1:p.Ala299=
XM_011545962.2:c.*143T>C	XP_011544264.1:n.*143T>C
XM_017023732.1:c.*143T>C	XP_016879221.1:n.*143T>C
NM_025193.4:c.897T>C MANE Select	NP_079469.2:p.Ala299=
NM_001142777.2:c.*143T>C	NP_001136249.1:n.*143T>C
NM_001142778.2:c.*143T>C	NP_001136250.1:n.*143T>C