Canonical Allele Identifier: CA7925569

Gene: ABCC6

Linked Data

• ClinVar Variation Id: 372295
• ClinVar RCV Id: RCV000413984 ; RCV000499335 ; RCV002481269 ; RCV004530508
• dbSNP Id: rs63750457
• ExAC: 16:16256865 C / T
• gnomAD v2: 16-16256865-C-T
• gnomAD v3: 16-16163008-C-T
• gnomAD v4: 16-16163008-C-T
• MyVariant Identifiers: chr16:g.16256865C>T (hg19) ; chr16:g.16163008C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163008C>T , CM000678.2:g.16163008C>T	GRCh38
NC_000016.9:g.16256865C>T , CM000678.1:g.16256865C>T	GRCh37
NC_000016.8:g.16164366C>T	NCBI36
NG_007558.2:g.65464G>A
NG_007558.3:g.65610G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3491G>A	ENSP00000483331.2:p.Arg1164Gln
ENST00000205557.12:c.3491G>A MANE Select	ENSP00000205557.7:p.Arg1164Gln
ENST00000640696.1:c.321-1444G>A	ENSP00000492197.1:n.321-1444G>A
ENST00000205557.11:c.3491G>A	ENSP00000205557.7:p.Arg1164Gln
ENST00000456970.6:c.3132-1444G>A	ENSP00000405002.2:n.3132-1444G>A
ENST00000622290.4:c.*700G>A	ENSP00000483331.1:n.*700G>A
NM_001171.5:c.3491G>A	NP_001162.4:p.Arg1164Gln
XM_011522479.1:c.3458G>A	XP_011520781.1:p.Arg1153Gln
XM_011522480.1:c.3149G>A	XP_011520782.1:p.Arg1050Gln
XM_011522481.1:c.3149G>A	XP_011520783.1:p.Arg1050Gln
XR_932836.1:n.3726G>A
XR_932837.1:n.3543-1444G>A
XR_932838.1:n.3543-1444G>A
XR_933133.1:n.407+165C>T
XR_933134.1:n.754+165C>T
NM_001351800.1:c.3149G>A	NP_001338729.1:p.Arg1050Gln
NR_147784.1:n.3169-1444G>A
XM_011522479.2:c.3458G>A	XP_011520781.1:p.Arg1153Gln
XM_011522481.3:c.3149G>A	XP_011520783.1:p.Arg1050Gln
XM_017023212.1:c.3323G>A	XP_016878701.1:p.Arg1108Gln
XM_017023214.1:c.3307-1444G>A	XP_016878703.1:n.3307-1444G>A
XM_024450261.1:c.3527G>A	XP_024306029.1:p.Arg1176Gln
XR_932836.2:n.3672G>A
XR_932837.3:n.3488-1444G>A
XR_932838.3:n.3488-1444G>A
NM_001171.6:c.3491G>A MANE Select	NP_001162.5:p.Arg1164Gln