Canonical Allele Identifier: CA2780626413
Gene: CYP7B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64727528A>C , CM000670.2:g.64727528A>C GRCh38
NC_000008.10:g.65640085A>C , CM000670.1:g.65640085A>C GRCh37
NC_000008.9:g.65802639A>C NCBI36
NG_008338.1:g.76264T>G
NG_008338.2:g.76264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.122+70938T>G MANE Select ENSP00000310721.3:n.122+70938T>G
ENST00000310193.3:c.122+70938T>G ENSP00000310721.3:n.122+70938T>G
NM_004820.3:c.122+70938T>G NP_004811.1:n.122+70938T>G
NM_001324112.1:c.122+70938T>G NP_001311041.1:n.122+70938T>G
NM_004820.4:c.122+70938T>G NP_004811.1:n.122+70938T>G
NM_004820.5:c.122+70938T>G MANE Select NP_004811.1:n.122+70938T>G
NM_001324112.2:c.122+70938T>G NP_001311041.1:n.122+70938T>G
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