Canonical Allele Identifier: CA2658668442
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076414-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076414A>C , CM000664.2:g.38076414A>C GRCh38
NC_000002.11:g.38303556A>C , CM000664.1:g.38303556A>C GRCh37
NC_000002.10:g.38157060A>C NCBI36
NG_008386.2:g.4688T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-5104T>G ENSP00000479876.1:n.-70-5104T>G
XM_011533236.1:c.1028A>C XP_011531538.1:p.His343Pro