Canonical Allele Identifier: CA715672137
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1401195872
MyVariant Identifiers: chr15:g.75041429G>T (hg19) chr15:g.74749088G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749088G>T , CM000677.2:g.74749088G>T GRCh38
NC_000015.9:g.75041429G>T , CM000677.1:g.75041429G>T GRCh37
NC_000015.8:g.72828482G>T NCBI36
NG_008431.1:g.31547G>T
NG_008431.2:g.31547G>T
NG_061543.1:g.5244G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-10+191G>T MANE Select ENSP00000342007.4:n.-10+191G>T
ENST00000343932.4:c.-10+191G>T ENSP00000342007.4:n.-10+191G>T
NM_000761.4:c.-10+191G>T NP_000752.2:n.-10+191G>T
NM_000761.5:c.-10+191G>T MANE Select NP_000752.2:n.-10+191G>T
Search 100 bp 5'
Search 100 bp 3'