Canonical Allele Identifier: CA7660037
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs528804804
ExAC: 15:75045582 C / T
gnomAD v2: 15-75045582-C-T
gnomAD v3: 15-74753241-C-T
gnomAD v4: 15-74753241-C-T
MyVariant Identifiers: chr15:g.75045582C>T (hg19) chr15:g.74753241C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753241C>T , CM000677.2:g.74753241C>T GRCh38
NC_000015.9:g.75045582C>T , CM000677.1:g.75045582C>T GRCh37
NC_000015.8:g.72832635C>T NCBI36
NG_008431.1:g.35700C>T
NG_008431.2:g.35700C>T
NG_061543.1:g.9397C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1224C>T MANE Select ENSP00000342007.4:p.Phe408=
ENST00000343932.4:c.1224C>T ENSP00000342007.4:p.Phe408=
NM_000761.4:c.1224C>T NP_000752.2:p.Phe408=
NM_000761.5:c.1224C>T MANE Select NP_000752.2:p.Phe408=
Search 100 bp 5'
Search 100 bp 3'