Canonical Allele Identifier: CA358950280

Gene: CYP4V2

Linked Data

• dbSNP Id: rs777857814
• gnomAD v3: 4-186208976-G-C
• gnomAD v4: 4-186208976-G-C
• MyVariant Identifiers: chr4:g.187130130G>C (hg19) ; chr4:g.186208976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208976G>C , CM000666.2:g.186208976G>C	GRCh38
NC_000004.11:g.187130130G>C , CM000666.1:g.187130130G>C	GRCh37
NC_000004.10:g.187367124G>C	NCBI36
NG_007965.1:g.22457G>C
NG_012095.2:g.4998G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1202G>C MANE Select	ENSP00000368079.4:p.Ser401Thr
ENST00000378802.4:c.1202G>C	ENSP00000368079.4:p.Ser401Thr
ENST00000502665.1:n.437G>C
ENST00000507209.5:n.5900G>C
ENST00000513354.5:n.292G>C
NM_207352.3:c.1202G>C	NP_997235.3:p.Ser401Thr
XM_005262935.2:c.1202G>C	XP_005262992.1:p.Ser401Thr
XM_006714184.2:c.806G>C	XP_006714247.1:p.Ser269Thr
XM_005262935.4:c.1202G>C	XP_005262992.1:p.Ser401Thr
XM_017008037.1:c.806G>C	XP_016863526.1:p.Ser269Thr
NM_207352.4:c.1202G>C MANE Select	NP_997235.3:p.Ser401Thr