Canonical Allele Identifier: CA280621851

Gene: VKORC1

Linked Data

• dbSNP Id: rs772725030
• gnomAD v2: 16-31105379-T-C
• gnomAD v3: 16-31094058-T-C
• gnomAD v4: 16-31094058-T-C
• MyVariant Identifiers: chr16:g.31105379T>C (hg19) ; chr16:g.31094058T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094058T>C , CM000678.2:g.31094058T>C	GRCh38
NC_000016.9:g.31105379T>C , CM000678.1:g.31105379T>C	GRCh37
NC_000016.8:g.31012880T>C	NCBI36
NG_011564.1:g.5898A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.173+499A>G MANE Select	ENSP00000378426.2:n.173+499A>G
ENST00000300851.10:c.173+499A>G	ENSP00000300851.6:n.173+499A>G
ENST00000319788.11:c.173+499A>G	ENSP00000326135.7:n.173+499A>G
ENST00000354895.4:c.173+499A>G	ENSP00000346969.4:n.173+499A>G
ENST00000394971.7:c.267+177A>G	ENSP00000378422.3:n.267+177A>G
ENST00000394975.2:c.173+499A>G	ENSP00000378426.2:n.173+499A>G
ENST00000420057.2:c.245+1331A>G
ENST00000498155.1:c.271-637A>G	ENSP00000417662.1:n.271-637A>G
ENST00000529564.1:c.173+499A>G	ENSP00000431371.1:n.173+499A>G
ENST00000532364.1:c.173+499A>G	ENSP00000460316.1:n.173+499A>G
ENST00000533518.5:c.46+499A>G
NM_001311311.1:c.173+499A>G	NP_001298240.1:n.173+499A>G
NM_024006.4:c.173+499A>G	NP_076869.1:n.173+499A>G
NM_024006.5:c.173+499A>G	NP_076869.1:n.173+499A>G
NM_206824.1:c.173+499A>G	NP_996560.1:n.173+499A>G
NM_206824.2:c.173+499A>G	NP_996560.1:n.173+499A>G
XM_011545944.1:c.173+499A>G	XP_011544246.1:n.173+499A>G
XM_011545945.1:c.173+499A>G	XP_011544247.1:n.173+499A>G
XR_950848.1:n.961+499A>G
NM_024006.6:c.173+499A>G MANE Select	NP_076869.1:n.173+499A>G
NM_001311311.2:c.173+499A>G	NP_001298240.1:n.173+499A>G
NM_206824.3:c.173+499A>G	NP_996560.1:n.173+499A>G