Canonical Allele Identifier: CA371334305

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65517388G>T (hg19) ; chr8:g.64604831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604831G>T , CM000670.2:g.64604831G>T	GRCh38
NC_000008.10:g.65517388G>T , CM000670.1:g.65517388G>T	GRCh37
NC_000008.9:g.65679942G>T	NCBI36
NG_008338.1:g.198961C>A
NG_008338.2:g.198961C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1084C>A MANE Select	ENSP00000310721.3:p.Leu362Met
ENST00000310193.3:c.1084C>A	ENSP00000310721.3:p.Leu362Met
ENST00000523954.1:n.358C>A
NM_004820.3:c.1084C>A	NP_004811.1:p.Leu362Met
NM_001324112.1:c.1084C>A	NP_001311041.1:p.Leu362Met
NM_004820.4:c.1084C>A	NP_004811.1:p.Leu362Met
XM_017014002.1:c.1150C>A	XP_016869491.1:p.Leu384Met
NM_004820.5:c.1084C>A MANE Select	NP_004811.1:p.Leu362Met
NM_001324112.2:c.1084C>A	NP_001311041.1:p.Leu362Met