Canonical Allele Identifier: CA2672897379
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186197329-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197329G>T , CM000666.2:g.186197329G>T GRCh38
NC_000004.11:g.187118483G>T , CM000666.1:g.187118483G>T GRCh37
NC_000004.10:g.187355477G>T NCBI36
NG_007965.1:g.10810G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.604+199G>T MANE Select ENSP00000368079.4:n.604+199G>T
ENST00000378802.4:c.604+199G>T ENSP00000368079.4:n.604+199G>T
ENST00000507209.5:n.1242G>T
NM_207352.3:c.604+199G>T NP_997235.3:n.604+199G>T
XM_005262935.2:c.604+199G>T XP_005262992.1:n.604+199G>T
XM_006714184.2:c.208+199G>T XP_006714247.1:n.208+199G>T
XM_005262935.4:c.604+199G>T XP_005262992.1:n.604+199G>T
XM_017008037.1:c.208+199G>T XP_016863526.1:n.208+199G>T
NM_207352.4:c.604+199G>T MANE Select NP_997235.3:n.604+199G>T
Search 100 bp 5'
Search 100 bp 3'