Canonical Allele Identifier: CA358942064

Gene: F11

Linked Data

• dbSNP Id: rs121965071
• gnomAD v2: 4-187205363-G-C
• gnomAD v4: 4-186284209-G-C
• MyVariant Identifiers: chr4:g.187205363G>C (hg19) ; chr4:g.186284209G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284209G>C , CM000666.2:g.186284209G>C	GRCh38
NC_000004.11:g.187205363G>C , CM000666.1:g.187205363G>C	GRCh37
NC_000004.10:g.187442357G>C	NCBI36
NG_008051.1:g.23246G>C , LRG_583:g.23246G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1253G>C MANE Select	ENSP00000384957.2:p.Gly418Ala
ENST00000264692.8:c.1091G>C	ENSP00000264692.5:p.Gly364Ala
ENST00000403665.6:c.1253G>C	ENSP00000384957.2:p.Gly418Ala
NM_000128.3:c.1253G>C , LRG_583t1:c.1253G>C	NP_000119.1:p.Gly418Ala
XM_005262821.2:c.1256G>C	XP_005262878.1:p.Gly419Ala
XM_005262822.2:c.1256G>C	XP_005262879.1:p.Gly419Ala
XM_005262823.2:c.986G>C	XP_005262880.1:p.Gly329Ala
XM_005262824.1:c.1256G>C	XP_005262881.1:p.Gly419Ala
XM_006714137.1:c.1208G>C	XP_006714200.1:p.Gly403Ala
XR_938706.1:n.1661G>C
XR_938707.1:n.1661G>C
XM_005262821.4:c.1256G>C	XP_005262878.1:p.Gly419Ala
XM_005262822.4:c.1256G>C	XP_005262879.1:p.Gly419Ala
XM_005262823.4:c.986G>C	XP_005262880.1:p.Gly329Ala
XM_006714137.3:c.1208G>C	XP_006714200.1:p.Gly403Ala
XR_001741172.2:n.1727G>C
NM_000128.4:c.1253G>C MANE Select	NP_000119.1:p.Gly418Ala