Canonical Allele Identifier: CA395642938

Gene: HSD3B7

Linked Data

• MyVariant Identifiers: chr16:g.30999196T>G (hg19) ; chr16:g.30987875T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30987875T>G , CM000678.2:g.30987875T>G	GRCh38
NC_000016.9:g.30999196T>G , CM000678.1:g.30999196T>G	GRCh37
NC_000016.8:g.30906697T>G	NCBI36
NG_012346.1:g.7678T>G
NG_041829.1:g.27634A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.802T>G MANE Select	ENSP00000297679.5:p.Tyr268Asp
ENST00000262520.10:c.*48T>G	ENSP00000262520.6:n.*48T>G
ENST00000297679.9:c.802T>G	ENSP00000297679.5:p.Tyr268Asp
NM_001142777.1:c.*48T>G	NP_001136249.1:n.*48T>G
NM_001142778.1:c.*48T>G	NP_001136250.1:n.*48T>G
NM_025193.3:c.802T>G	NP_079469.2:p.Tyr268Asp
XM_005255601.3:c.802T>G	XP_005255658.2:p.Tyr268Asp
XM_011545960.1:c.802T>G	XP_011544262.1:p.Tyr268Asp
XM_011545961.1:c.802T>G	XP_011544263.1:p.Tyr268Asp
XM_011545962.1:c.*48T>G	XP_011544264.1:n.*48T>G
XM_011545960.2:c.802T>G	XP_011544262.1:p.Tyr268Asp
XM_011545962.2:c.*48T>G	XP_011544264.1:n.*48T>G
XM_017023732.1:c.*48T>G	XP_016879221.1:n.*48T>G
NM_025193.4:c.802T>G MANE Select	NP_079469.2:p.Tyr268Asp
NM_001142777.2:c.*48T>G	NP_001136249.1:n.*48T>G
NM_001142778.2:c.*48T>G	NP_001136250.1:n.*48T>G