Canonical Allele Identifier: CA1245628773
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1682537272
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076199A>T , CM000664.2:g.38076199A>T GRCh38
NC_000002.11:g.38303341A>T , CM000664.1:g.38303341A>T GRCh37
NC_000002.10:g.38156845A>T NCBI36
NG_008386.2:g.4903T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-4889T>A ENSP00000479876.1:n.-70-4889T>A
XM_011533236.1:c.813A>T XP_011531538.1:p.Gly271=
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