Canonical Allele Identifier: CA792315629
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs929171098
gnomAD v4: 4-186191708-G-T
MyVariant Identifiers: chr4:g.187112862G>T (hg19) chr4:g.186191708G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191708G>T , CM000666.2:g.186191708G>T GRCh38
NC_000004.11:g.187112862G>T , CM000666.1:g.187112862G>T GRCh37
NC_000004.10:g.187349856G>T NCBI36
NG_007965.1:g.5189G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-116G>T MANE Select ENSP00000368079.4:n.-116G>T
ENST00000378802.4:c.-116G>T ENSP00000368079.4:n.-116G>T
NM_207352.3:c.-116G>T NP_997235.3:n.-116G>T
XM_005262935.2:c.-116G>T XP_005262992.1:n.-116G>T
XM_017008037.1:c.-426G>T XP_016863526.1:n.-426G>T
NM_207352.4:c.-116G>T MANE Select NP_997235.3:n.-116G>T
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