Canonical Allele Identifier: CA1789659741
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604836A= , CM000670.2:g.64604836A= GRCh38
NC_000008.10:g.65517393A= , CM000670.1:g.65517393A= GRCh37
NC_000008.9:g.65679947A= NCBI36
NG_008338.1:g.198956T=
NG_008338.2:g.198956T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1079T= MANE Select ENSP00000310721.3:p.Leu360=
ENST00000310193.3:c.1079T= ENSP00000310721.3:p.Leu360=
ENST00000523954.1:n.353T=
NM_004820.3:c.1079T= NP_004811.1:p.Leu360=
NM_001324112.1:c.1079T= NP_001311041.1:p.Leu360=
NM_004820.4:c.1079T= NP_004811.1:p.Leu360=
XM_017014002.1:c.1145T= XP_016869491.1:p.Leu382=
NM_004820.5:c.1079T= MANE Select NP_004811.1:p.Leu360=
NM_001324112.2:c.1079T= NP_001311041.1:p.Leu360=