Canonical Allele Identifier: CA2187824231
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063301250

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748984G>T , CM000677.2:g.74748984G>T GRCh38
NC_000015.9:g.75041325G>T , CM000677.1:g.75041325G>T GRCh37
NC_000015.8:g.72828378G>T NCBI36
NG_008431.1:g.31443G>T
NG_008431.2:g.31443G>T
NG_061543.1:g.5140G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+87G>T MANE Select ENSP00000342007.4:n.-10+87G>T
ENST00000343932.4:c.-10+87G>T ENSP00000342007.4:n.-10+87G>T
NM_000761.4:c.-10+87G>T NP_000752.2:n.-10+87G>T
NM_000761.5:c.-10+87G>T MANE Select NP_000752.2:n.-10+87G>T