Canonical Allele Identifier: CA842281022

Gene: POR

Linked Data

• dbSNP Id: rs1443411721
• MyVariant Identifiers: chr7:g.75984614C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.75984614C>T , CM000669.2:g.75984614C>T	GRCh38
NC_000007.13:g.75613932C>T , CM000669.1:g.75613932C>T	GRCh37
NC_000007.12:g.75451868C>T	NCBI36
NG_008930.1:g.74513C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475509.2:c.842-163C>T	ENSP00000516446.1:n.842-163C>T
ENST00000706544.1:c.968-163C>T	ENSP00000516442.1:n.968-163C>T
ENST00000706545.1:c.1067-163C>T	ENSP00000516443.1:n.1067-163C>T
ENST00000706546.1:c.1067-163C>T	ENSP00000516444.1:n.1067-163C>T
ENST00000706547.1:c.1067-163C>T	ENSP00000516445.1:n.1067-163C>T
ENST00000461988.6:c.1067-163C>T MANE Select	ENSP00000419970.1:n.1067-163C>T
ENST00000394893.5:c.1067-163C>T	ENSP00000378355.1:n.1067-163C>T
ENST00000412064.6:c.*108+978C>T	ENSP00000404731.2:n.*108+978C>T
ENST00000439269.1:c.281-163C>T	ENSP00000412490.1:n.281-163C>T
ENST00000447222.5:c.1218-163C>T
ENST00000454934.5:c.*372-163C>T	ENSP00000414263.1:n.*372-163C>T
ENST00000461988.5:c.1067-163C>T	ENSP00000419970.1:n.1067-163C>T
ENST00000487247.5:n.422-163C>T
ENST00000495770.1:n.69-163C>T
ENST00000496888.5:n.441-163C>T
NM_000941.2:c.1067-163C>T	NP_000932.3:n.1067-163C>T
NM_000941.3:c.1067-163C>T	NP_000932.3:n.1067-163C>T
NM_001367562.1:c.1067-163C>T	NP_001354491.1:n.1067-163C>T
NM_001382655.1:c.1121-163C>T	NP_001369584.1:n.1121-163C>T
NM_001382657.1:c.1067-163C>T	NP_001369586.1:n.1067-163C>T
NM_001382658.1:c.1067-163C>T	NP_001369587.1:n.1067-163C>T
NM_001382659.1:c.1067-163C>T	NP_001369588.1:n.1067-163C>T
NM_001382662.1:c.1067-163C>T	NP_001369591.1:n.1067-163C>T
NM_001367562.3:c.1058-163C>T	NP_001354491.2:n.1058-163C>T
NM_001382655.3:c.1112-163C>T	NP_001369584.2:n.1112-163C>T
NM_001382657.2:c.1058-163C>T	NP_001369586.2:n.1058-163C>T
NM_001382658.3:c.1058-163C>T	NP_001369587.2:n.1058-163C>T
NM_001382659.3:c.1058-163C>T	NP_001369588.2:n.1058-163C>T
NM_001382662.3:c.1058-163C>T	NP_001369591.2:n.1058-163C>T
NM_001395413.1:c.1058-163C>T MANE Select	NP_001382342.1:n.1058-163C>T