Canonical Allele Identifier: CA2658668427
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076402-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076402G>A , CM000664.2:g.38076402G>A GRCh38
NC_000002.11:g.38303544G>A , CM000664.1:g.38303544G>A GRCh37
NC_000002.10:g.38157048G>A NCBI36
NG_008386.2:g.4700C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-5092C>T ENSP00000479876.1:n.-70-5092C>T
XM_011533236.1:c.1016G>A XP_011531538.1:p.Cys339Tyr