Canonical Allele Identifier: CA2658668437
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076411-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076411A>G , CM000664.2:g.38076411A>G GRCh38
NC_000002.11:g.38303553A>G , CM000664.1:g.38303553A>G GRCh37
NC_000002.10:g.38157057A>G NCBI36
NG_008386.2:g.4691T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-5101T>C ENSP00000479876.1:n.-70-5101T>C
XM_011533236.1:c.1025A>G XP_011531538.1:p.Asn342Ser
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