Canonical Allele Identifier: CA395640508

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30997942C>A (hg19) ; chr16:g.30986621C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986621C>A , CM000678.2:g.30986621C>A	GRCh38
NC_000016.9:g.30997942C>A , CM000678.1:g.30997942C>A	GRCh37
NC_000016.8:g.30905443C>A	NCBI36
NG_012346.1:g.6424C>A
NG_052948.1:g.34328C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297679.10:c.448C>A MANE Select	ENSP00000297679.5:p.Pro150Thr
ENST00000262520.10:c.448C>A	ENSP00000262520.6:p.Pro150Thr
ENST00000297679.9:c.448C>A	ENSP00000297679.5:p.Pro150Thr
ENST00000562932.5:c.571C>A	ENSP00000459852.1:p.Pro191Thr
ENST00000574447.1:c.448C>A	ENSP00000459689.1:p.Pro150Thr
NM_001142777.1:c.448C>A	NP_001136249.1:p.Pro150Thr
NM_001142778.1:c.448C>A	NP_001136250.1:p.Pro150Thr
NM_025193.3:c.448C>A	NP_079469.2:p.Pro150Thr
XM_005255601.3:c.448C>A	XP_005255658.2:p.Pro150Thr
XM_011545960.1:c.448C>A	XP_011544262.1:p.Pro150Thr
XM_011545961.1:c.448C>A	XP_011544263.1:p.Pro150Thr
XM_011545962.1:c.448C>A	XP_011544264.1:p.Pro150Thr
XM_011545960.2:c.448C>A	XP_011544262.1:p.Pro150Thr
XM_011545962.2:c.448C>A	XP_011544264.1:p.Pro150Thr
XM_017023732.1:c.448C>A	XP_016879221.1:p.Pro150Thr
NM_025193.4:c.448C>A MANE Select	NP_079469.2:p.Pro150Thr
NM_001142777.2:c.448C>A	NP_001136249.1:p.Pro150Thr
NM_001142778.2:c.448C>A	NP_001136250.1:p.Pro150Thr