Canonical Allele Identifier: CA491489605
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042550C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750209C>G , CM000677.2:g.74750209C>G GRCh38
NC_000015.9:g.75042550C>G , CM000677.1:g.75042550C>G GRCh37
NC_000015.8:g.72829603C>G NCBI36
NG_008431.1:g.32668C>G
NG_008431.2:g.32668C>G
NG_061543.1:g.6365C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.471C>G MANE Select ENSP00000342007.4:p.Ser157=
ENST00000343932.4:c.471C>G ENSP00000342007.4:p.Ser157=
NM_000761.4:c.471C>G NP_000752.2:p.Ser157=
NM_000761.5:c.471C>G MANE Select NP_000752.2:p.Ser157=
Search 100 bp 5'
Search 100 bp 3'