Canonical Allele Identifier: CA1789668083

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624606_64624607delinsTG , CM000670.2:g.64624606_64624607delinsTG	GRCh38
NC_000008.10:g.65537163_65537164delinsTG , CM000670.1:g.65537163_65537164delinsTG	GRCh37
NC_000008.9:g.65699717_65699718delinsTG	NCBI36
NG_008338.1:g.179185_179186delinsCA
NG_008338.2:g.179185_179186delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.123-68_123-67delinsCA MANE Select	ENSP00000310721.3:n.123-68_123-67delinsCA
ENST00000310193.3:c.123-68_123-67delinsCA	ENSP00000310721.3:n.123-68_123-67delinsCA
NM_004820.3:c.123-68_123-67delinsCA	NP_004811.1:n.123-68_123-67delinsCA
NM_001324112.1:c.123-68_123-67delinsCA	NP_001311041.1:n.123-68_123-67delinsCA
NM_004820.4:c.123-68_123-67delinsCA	NP_004811.1:n.123-68_123-67delinsCA
XM_017014002.1:c.189-68_189-67delinsCA	XP_016869491.1:n.189-68_189-67delinsCA
NM_004820.5:c.123-68_123-67delinsCA MANE Select	NP_004811.1:n.123-68_123-67delinsCA
NM_001324112.2:c.123-68_123-67delinsCA	NP_001311041.1:n.123-68_123-67delinsCA