Canonical Allele Identifier: CA473871942

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46749684G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728134G>C , CM000673.2:g.46728134G>C	GRCh38
NC_000011.9:g.46749684G>C , CM000673.1:g.46749684G>C	GRCh37
NC_000011.8:g.46706260G>C	NCBI36
NG_008953.1:g.13942G>C , LRG_551:g.13942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1269G>C MANE Select	ENSP00000308541.5:p.Leu423=
ENST00000311907.9:c.1269G>C	ENSP00000308541.5:p.Leu423=
ENST00000530231.5:c.1269G>C	ENSP00000433907.1:p.Leu423=
NM_000506.3:c.1269G>C	NP_000497.1:p.Leu423=
NM_000506.4:c.1269G>C , LRG_551t1:c.1269G>C	NP_000497.1:p.Leu423=
NM_001311257.1:c.1221G>C	NP_001298186.1:p.Leu407=
XR_428840.2:n.1313G>C
XR_428840.4:n.1304G>C
NM_000506.5:c.1269G>C MANE Select	NP_000497.1:p.Leu423=
NM_001311257.2:c.1221G>C	NP_001298186.1:p.Leu407=