Canonical Allele Identifier: CA393178089
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042380C>T (hg19) chr15:g.74750039C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750039C>T , CM000677.2:g.74750039C>T GRCh38
NC_000015.9:g.75042380C>T , CM000677.1:g.75042380C>T GRCh37
NC_000015.8:g.72829433C>T NCBI36
NG_008431.1:g.32498C>T
NG_008431.2:g.32498C>T
NG_061543.1:g.6195C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.301C>T MANE Select ENSP00000342007.4:p.Gln101Ter
ENST00000343932.4:c.301C>T ENSP00000342007.4:p.Gln101Ter
NM_000761.4:c.301C>T NP_000752.2:p.Gln101Ter
NM_000761.5:c.301C>T MANE Select NP_000752.2:p.Gln101Ter
Search 100 bp 5'
Search 100 bp 3'