Canonical Allele Identifier: CA405965121
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848227-T-C
MyVariant Identifiers: chr19:g.41354132T>C (hg19) chr19:g.40848227T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848227T>C , CM000681.2:g.40848227T>C GRCh38
NC_000019.9:g.41354132T>C , CM000681.1:g.41354132T>C GRCh37
NC_000019.8:g.46045972T>C NCBI36
NG_008377.1:g.7221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.646A>G MANE Select ENSP00000301141.4:p.Thr216Ala
ENST00000301141.9:c.646A>G ENSP00000301141.4:p.Thr216Ala
ENST00000596719.5:n.497A>G
ENST00000600495.1:c.*458A>G ENSP00000472905.1:n.*458A>G
ENST00000601627.1:c.120-43764T>C
ENST00000610301.1:c.646A>G ENSP00000477899.1:p.Thr216Ala
NM_000762.5:c.646A>G NP_000753.3:p.Thr216Ala
NM_000762.6:c.646A>G MANE Select NP_000753.3:p.Thr216Ala
Search 100 bp 5'
Search 100 bp 3'