Canonical Allele Identifier: CA494920677
Gene: HSD3B7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30997944A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986623A>G , CM000678.2:g.30986623A>G GRCh38
NC_000016.9:g.30997944A>G , CM000678.1:g.30997944A>G GRCh37
NC_000016.8:g.30905445A>G NCBI36
NG_012346.1:g.6426A>G
NG_052948.1:g.34330A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297679.10:c.450A>G MANE Select ENSP00000297679.5:p.Pro150=
ENST00000262520.10:c.450A>G ENSP00000262520.6:p.Pro150=
ENST00000297679.9:c.450A>G ENSP00000297679.5:p.Pro150=
ENST00000562932.5:c.573A>G ENSP00000459852.1:p.Pro191=
ENST00000574447.1:c.450A>G ENSP00000459689.1:p.Pro150=
NM_001142777.1:c.450A>G NP_001136249.1:p.Pro150=
NM_001142778.1:c.450A>G NP_001136250.1:p.Pro150=
NM_025193.3:c.450A>G NP_079469.2:p.Pro150=
XM_005255601.3:c.450A>G XP_005255658.2:p.Pro150=
XM_011545960.1:c.450A>G XP_011544262.1:p.Pro150=
XM_011545961.1:c.450A>G XP_011544263.1:p.Pro150=
XM_011545962.1:c.450A>G XP_011544264.1:p.Pro150=
XM_011545960.2:c.450A>G XP_011544262.1:p.Pro150=
XM_011545962.2:c.450A>G XP_011544264.1:p.Pro150=
XM_017023732.1:c.450A>G XP_016879221.1:p.Pro150=
NM_025193.4:c.450A>G MANE Select NP_079469.2:p.Pro150=
NM_001142777.2:c.450A>G NP_001136249.1:p.Pro150=
NM_001142778.2:c.450A>G NP_001136250.1:p.Pro150=