Canonical Allele Identifier: CA272815212
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1002092168
gnomAD v4: 15-74751943-T-G
MyVariant Identifiers: chr15:g.75044284T>G (hg19) chr15:g.74751943T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751943T>G , CM000677.2:g.74751943T>G GRCh38
NC_000015.9:g.75044284T>G , CM000677.1:g.75044284T>G GRCh37
NC_000015.8:g.72831337T>G NCBI36
NG_008431.1:g.34402T>G
NG_008431.2:g.34402T>G
NG_061543.1:g.8099T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+89T>G MANE Select ENSP00000342007.4:n.1042+89T>G
ENST00000343932.4:c.1042+89T>G ENSP00000342007.4:n.1042+89T>G
NM_000761.4:c.1042+89T>G NP_000752.2:n.1042+89T>G
NM_000761.5:c.1042+89T>G MANE Select NP_000752.2:n.1042+89T>G
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