Canonical Allele Identifier: CA405961928
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41351236T>G (hg19) chr19:g.40845331T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845331T>G , CM000681.2:g.40845331T>G GRCh38
NC_000019.9:g.41351236T>G , CM000681.1:g.41351236T>G GRCh37
NC_000019.8:g.46043076T>G NCBI36
NG_008377.1:g.10117A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1124A>C MANE Select ENSP00000301141.4:p.Lys375Thr
ENST00000301141.9:c.1124A>C ENSP00000301141.4:p.Lys375Thr
ENST00000596719.5:n.975A>C
ENST00000601627.1:c.119+43916T>G
ENST00000610301.1:c.1124A>C ENSP00000477899.1:p.Lys375Thr
NM_000762.5:c.1124A>C NP_000753.3:p.Lys375Thr
NM_000762.6:c.1124A>C MANE Select NP_000753.3:p.Lys375Thr
Search 100 bp 5'
Search 100 bp 3'