Canonical Allele Identifier: CA371335903
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64616165T>C , CM000670.2:g.64616165T>C GRCh38
NC_000008.10:g.65528722T>C , CM000670.1:g.65528722T>C GRCh37
NC_000008.9:g.65691276T>C NCBI36
NG_008338.1:g.187627A>G
NG_008338.2:g.187627A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.376A>G MANE Select ENSP00000310721.3:p.Ser126Gly
ENST00000310193.3:c.376A>G ENSP00000310721.3:p.Ser126Gly
NM_004820.3:c.376A>G NP_004811.1:p.Ser126Gly
NM_001324112.1:c.376A>G NP_001311041.1:p.Ser126Gly
NM_004820.4:c.376A>G NP_004811.1:p.Ser126Gly
XM_017014002.1:c.442A>G XP_016869491.1:p.Ser148Gly
NM_004820.5:c.376A>G MANE Select NP_004811.1:p.Ser126Gly
NM_001324112.2:c.376A>G NP_001311041.1:p.Ser126Gly