Canonical Allele Identifier: CA7659932
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs778097570
ExAC: 15:75044124 C / G
gnomAD v2: 15-75044124-C-G
gnomAD v3: 15-74751783-C-G
gnomAD v4: 15-74751783-C-G
MyVariant Identifiers: chr15:g.75044124C>G (hg19) chr15:g.74751783C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751783C>G , CM000677.2:g.74751783C>G GRCh38
NC_000015.9:g.75044124C>G , CM000677.1:g.75044124C>G GRCh37
NC_000015.8:g.72831177C>G NCBI36
NG_008431.1:g.34242C>G
NG_008431.2:g.34242C>G
NG_061543.1:g.7939C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.971C>G MANE Select ENSP00000342007.4:p.Thr324Arg
ENST00000343932.4:c.971C>G ENSP00000342007.4:p.Thr324Arg
NM_000761.4:c.971C>G NP_000752.2:p.Thr324Arg
NM_000761.5:c.971C>G MANE Select NP_000752.2:p.Thr324Arg
Search 100 bp 5'
Search 100 bp 3'