Canonical Allele Identifier: CA324664031

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1555888328
• MyVariant Identifiers: chr22:g.42522138_42522139insTGT (hg19) ; chr22:g.42126136_42126137insTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126136_42126137insTGT , CM000684.2:g.42126136_42126137insTGT	GRCh38
NC_000022.10:g.42522138_42522139insTGT , CM000684.1:g.42522138_42522139insTGT	GRCh37
NC_000022.9:g.40852082_40852083insTGT	NCBI36
NG_008376.3:g.8856_8857insCAA
NG_008376.4:g.9675_9676insCAA

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.1453-183_1453-182insCAA	XP_011528268.1:n.1453-183_1453-182insCAA
XM_011529967.1:c.1453-183_1453-182insCAA	XP_011528269.1:n.1453-183_1453-182insCAA
XM_011529968.1:c.1453-209_1453-208insCAA	XP_011528270.1:n.1453-209_1453-208insCAA
XM_011529969.1:c.1309-183_1309-182insCAA	XP_011528271.1:n.1309-183_1309-182insCAA
XM_011529970.1:c.1300-183_1300-182insCAA	XP_011528272.1:n.1300-183_1300-182insCAA