Canonical Allele Identifier: CA358946998

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187115749A>C (hg19) ; chr4:g.186194595A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194595A>C , CM000666.2:g.186194595A>C	GRCh38
NC_000004.11:g.187115749A>C , CM000666.1:g.187115749A>C	GRCh37
NC_000004.10:g.187352743A>C	NCBI36
NG_007965.1:g.8076A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.310A>C MANE Select	ENSP00000368079.4:p.Asn104His
ENST00000378802.4:c.310A>C	ENSP00000368079.4:p.Asn104His
NM_207352.3:c.310A>C	NP_997235.3:p.Asn104His
XM_005262935.2:c.310A>C	XP_005262992.1:p.Asn104His
XM_006714184.2:c.-1A>C	XP_006714247.1:n.-1A>C
XM_005262935.4:c.310A>C	XP_005262992.1:p.Asn104His
XM_017008037.1:c.-1A>C	XP_016863526.1:n.-1A>C
NM_207352.4:c.310A>C MANE Select	NP_997235.3:p.Asn104His