Canonical Allele Identifier: CA715671258
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1430249596
gnomAD v4: 15-74755287-G-T
MyVariant Identifiers: chr15:g.75047628G>T (hg19) chr15:g.74755287G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755287G>T , CM000677.2:g.74755287G>T GRCh38
NC_000015.9:g.75047628G>T , CM000677.1:g.75047628G>T GRCh37
NC_000015.8:g.72834681G>T NCBI36
NG_008431.1:g.37746G>T
NG_008431.2:g.37746G>T
NG_061543.1:g.11443G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*199G>T MANE Select ENSP00000342007.4:n.*199G>T
ENST00000343932.4:c.*199G>T ENSP00000342007.4:n.*199G>T
NM_000761.4:c.*199G>T NP_000752.2:n.*199G>T
NM_000761.5:c.*199G>T MANE Select NP_000752.2:n.*199G>T
Search 100 bp 5'
Search 100 bp 3'