Canonical Allele Identifier: CA3162781

Gene: CYP4V2

Linked Data

• dbSNP Id: rs758771290
• ExAC: 4:187130123 G / T
• gnomAD v2: 4-187130123-G-T
• gnomAD v3: 4-186208969-G-T
• gnomAD v4: 4-186208969-G-T
• MyVariant Identifiers: chr4:g.187130123G>T (hg19) ; chr4:g.186208969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208969G>T , CM000666.2:g.186208969G>T	GRCh38
NC_000004.11:g.187130123G>T , CM000666.1:g.187130123G>T	GRCh37
NC_000004.10:g.187367117G>T	NCBI36
NG_007965.1:g.22450G>T
NG_012095.2:g.4991G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1195G>T MANE Select	ENSP00000368079.4:p.Ala399Ser
ENST00000378802.4:c.1195G>T	ENSP00000368079.4:p.Ala399Ser
ENST00000502665.1:n.430G>T
ENST00000507209.5:n.5893G>T
ENST00000513354.5:n.285G>T
NM_207352.3:c.1195G>T	NP_997235.3:p.Ala399Ser
XM_005262935.2:c.1195G>T	XP_005262992.1:p.Ala399Ser
XM_006714184.2:c.799G>T	XP_006714247.1:p.Ala267Ser
XM_005262935.4:c.1195G>T	XP_005262992.1:p.Ala399Ser
XM_017008037.1:c.799G>T	XP_016863526.1:p.Ala267Ser
NM_207352.4:c.1195G>T MANE Select	NP_997235.3:p.Ala399Ser