Canonical Allele Identifier: CA394884450

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263566C>T (hg19) ; chr16:g.16169709C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169709C>T , CM000678.2:g.16169709C>T	GRCh38
NC_000016.9:g.16263566C>T , CM000678.1:g.16263566C>T	GRCh37
NC_000016.8:g.16171067C>T	NCBI36
NG_007558.2:g.58763G>A
NG_007558.3:g.58909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2932G>A	ENSP00000483331.2:p.Gly978Ser
ENST00000205557.12:c.2932G>A MANE Select	ENSP00000205557.7:p.Gly978Ser
ENST00000205557.11:c.2932G>A	ENSP00000205557.7:p.Gly978Ser
ENST00000456970.6:c.2757G>A	ENSP00000405002.2:n.2757G>A
ENST00000622290.4:c.*141G>A	ENSP00000483331.1:n.*141G>A
NM_001171.5:c.2932G>A	NP_001162.4:p.Gly978Ser
XM_011522479.1:c.2899G>A	XP_011520781.1:p.Gly967Ser
XM_011522480.1:c.2590G>A	XP_011520782.1:p.Gly864Ser
XM_011522481.1:c.2590G>A	XP_011520783.1:p.Gly864Ser
XR_932836.1:n.3167G>A
XR_932837.1:n.3168G>A
XR_932838.1:n.3168G>A
NM_001351800.1:c.2590G>A	NP_001338729.1:p.Gly864Ser
NR_147784.1:n.2794G>A
XM_011522479.2:c.2899G>A	XP_011520781.1:p.Gly967Ser
XM_011522481.3:c.2590G>A	XP_011520783.1:p.Gly864Ser
XM_017023212.1:c.2764G>A	XP_016878701.1:p.Gly922Ser
XM_017023214.1:c.2932G>A	XP_016878703.1:p.Gly978Ser
XM_024450261.1:c.2968G>A	XP_024306029.1:p.Gly990Ser
XR_932836.2:n.3113G>A
XR_932837.3:n.3113G>A
XR_932838.3:n.3113G>A
NM_001171.6:c.2932G>A MANE Select	NP_001162.5:p.Gly978Ser