Canonical Allele Identifier: CA1071991729

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736445643
• gnomAD v3: 4-186204779-A-T
• gnomAD v4: 4-186204779-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204779A>T , CM000666.2:g.186204779A>T	GRCh38
NC_000004.11:g.187125933A>T , CM000666.1:g.187125933A>T	GRCh37
NC_000004.10:g.187362927A>T	NCBI36
NG_007965.1:g.18260A>T
NG_012095.2:g.801A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-421A>T MANE Select	ENSP00000368079.4:n.988-421A>T
ENST00000378802.4:c.988-421A>T	ENSP00000368079.4:n.988-421A>T
ENST00000507209.5:n.5265A>T
ENST00000513354.5:n.77+322A>T
NM_207352.3:c.988-421A>T	NP_997235.3:n.988-421A>T
XM_005262935.2:c.988-421A>T	XP_005262992.1:n.988-421A>T
XM_006714184.2:c.592-421A>T	XP_006714247.1:n.592-421A>T
XM_005262935.4:c.988-421A>T	XP_005262992.1:n.988-421A>T
XM_017008037.1:c.592-421A>T	XP_016863526.1:n.592-421A>T
NM_207352.4:c.988-421A>T MANE Select	NP_997235.3:n.988-421A>T