Canonical Allele Identifier: CA395639631
Gene: HSD3B7 HGNC NCBI

Linked Data

dbSNP Id: rs1221763079

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986181C>T , CM000678.2:g.30986181C>T GRCh38
NC_000016.9:g.30997502C>T , CM000678.1:g.30997502C>T GRCh37
NC_000016.8:g.30905003C>T NCBI36
NG_012346.1:g.5984C>T
NG_052948.1:g.33888C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297679.10:c.299C>T MANE Select ENSP00000297679.5:p.Thr100Ile
ENST00000262520.10:c.299C>T ENSP00000262520.6:p.Thr100Ile
ENST00000297679.9:c.299C>T ENSP00000297679.5:p.Thr100Ile
ENST00000562932.5:c.422C>T ENSP00000459852.1:p.Thr141Ile
ENST00000574447.1:c.299C>T ENSP00000459689.1:p.Thr100Ile
NM_001142777.1:c.299C>T NP_001136249.1:p.Thr100Ile
NM_001142778.1:c.299C>T NP_001136250.1:p.Thr100Ile
NM_025193.3:c.299C>T NP_079469.2:p.Thr100Ile
XM_005255601.3:c.299C>T XP_005255658.2:p.Thr100Ile
XM_011545960.1:c.299C>T XP_011544262.1:p.Thr100Ile
XM_011545961.1:c.299C>T XP_011544263.1:p.Thr100Ile
XM_011545962.1:c.299C>T XP_011544264.1:p.Thr100Ile
XM_011545960.2:c.299C>T XP_011544262.1:p.Thr100Ile
XM_011545962.2:c.299C>T XP_011544264.1:p.Thr100Ile
XM_017023732.1:c.299C>T XP_016879221.1:p.Thr100Ile
NM_025193.4:c.299C>T MANE Select NP_079469.2:p.Thr100Ile
NM_001142777.2:c.299C>T NP_001136249.1:p.Thr100Ile
NM_001142778.2:c.299C>T NP_001136250.1:p.Thr100Ile