Canonical Allele Identifier: CA393179199
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74750277-T-G
MyVariant Identifiers: chr15:g.75042618T>G (hg19) chr15:g.74750277T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750277T>G , CM000677.2:g.74750277T>G GRCh38
NC_000015.9:g.75042618T>G , CM000677.1:g.75042618T>G GRCh37
NC_000015.8:g.72829671T>G NCBI36
NG_008431.1:g.32736T>G
NG_008431.2:g.32736T>G
NG_061543.1:g.6433T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.539T>G MANE Select ENSP00000342007.4:p.Met180Arg
ENST00000343932.4:c.539T>G ENSP00000342007.4:p.Met180Arg
NM_000761.4:c.539T>G NP_000752.2:p.Met180Arg
NM_000761.5:c.539T>G MANE Select NP_000752.2:p.Met180Arg
Search 100 bp 5'
Search 100 bp 3'