Canonical Allele Identifier: CA278670039
Gene: ABCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433206
dbSNP Id: rs72664281

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16214375C>T , CM000678.2:g.16214375C>T GRCh38
NC_000016.9:g.16308232C>T , CM000678.1:g.16308232C>T GRCh37
NC_000016.8:g.16215733C>T NCBI36
NG_007558.2:g.14097G>A
NG_007558.3:g.14243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.549G>A ENSP00000507301.1:p.Leu183=
ENST00000622290.5:c.549G>A ENSP00000483331.2:p.Leu183=
ENST00000205557.12:c.549G>A MANE Select ENSP00000205557.7:p.Leu183=
ENST00000205557.11:c.549G>A ENSP00000205557.7:p.Leu183=
ENST00000456970.6:c.549G>A ENSP00000405002.2:p.Leu183=
ENST00000574094.5:n.645G>A
ENST00000577103.1:c.*416G>A ENSP00000459243.1:n.*416G>A
ENST00000622290.4:c.549G>A ENSP00000483331.1:p.Leu183=
NM_001171.5:c.549G>A NP_001162.4:p.Leu183=
XM_011522479.1:c.549G>A XP_011520781.1:p.Leu183=
XM_011522480.1:c.207G>A XP_011520782.1:p.Leu69=
XM_011522481.1:c.207G>A XP_011520783.1:p.Leu69=
XM_011522482.1:c.549G>A XP_011520784.1:p.Leu183=
XR_932836.1:n.784G>A
XR_932837.1:n.785G>A
XR_932838.1:n.785G>A
XR_933132.1:n.381+2284C>T
NM_001351800.1:c.207G>A NP_001338729.1:p.Leu69=
NR_147784.1:n.586G>A
XM_011522479.2:c.549G>A XP_011520781.1:p.Leu183=
XM_011522481.3:c.207G>A XP_011520783.1:p.Leu69=
XM_011522482.3:c.549G>A XP_011520784.1:p.Leu183=
XM_017023212.1:c.549G>A XP_016878701.1:p.Leu183=
XM_017023214.1:c.549G>A XP_016878703.1:p.Leu183=
XM_024450261.1:c.585G>A XP_024306029.1:p.Leu195=
XR_001752340.1:n.596-876C>T
XR_001752341.1:n.595+1349C>T
XR_001752342.1:n.390-876C>T
XR_932836.2:n.730G>A
XR_932837.3:n.730G>A
XR_932838.3:n.730G>A
XR_933132.2:n.389+2284C>T
NM_001171.6:c.549G>A MANE Select NP_001162.5:p.Leu183=