Canonical Allele Identifier: CA394884476

Gene: ABCC6

Linked Data

• ClinVar Variation Id: 1501710
• ClinVar RCV Id: RCV002019884
• dbSNP Id: rs1310683915
• MyVariant Identifiers: chr16:g.16263572C>T (hg19) ; chr16:g.16169715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169715C>T , CM000678.2:g.16169715C>T	GRCh38
NC_000016.9:g.16263572C>T , CM000678.1:g.16263572C>T	GRCh37
NC_000016.8:g.16171073C>T	NCBI36
NG_007558.2:g.58757G>A
NG_007558.3:g.58903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2926G>A	ENSP00000483331.2:p.Ala976Thr
ENST00000205557.12:c.2926G>A MANE Select	ENSP00000205557.7:p.Ala976Thr
ENST00000205557.11:c.2926G>A	ENSP00000205557.7:p.Ala976Thr
ENST00000456970.6:c.2751G>A	ENSP00000405002.2:n.2751G>A
ENST00000622290.4:c.*135G>A	ENSP00000483331.1:n.*135G>A
NM_001171.5:c.2926G>A	NP_001162.4:p.Ala976Thr
XM_011522479.1:c.2893G>A	XP_011520781.1:p.Ala965Thr
XM_011522480.1:c.2584G>A	XP_011520782.1:p.Ala862Thr
XM_011522481.1:c.2584G>A	XP_011520783.1:p.Ala862Thr
XR_932836.1:n.3161G>A
XR_932837.1:n.3162G>A
XR_932838.1:n.3162G>A
NM_001351800.1:c.2584G>A	NP_001338729.1:p.Ala862Thr
NR_147784.1:n.2788G>A
XM_011522479.2:c.2893G>A	XP_011520781.1:p.Ala965Thr
XM_011522481.3:c.2584G>A	XP_011520783.1:p.Ala862Thr
XM_017023212.1:c.2758G>A	XP_016878701.1:p.Ala920Thr
XM_017023214.1:c.2926G>A	XP_016878703.1:p.Ala976Thr
XM_024450261.1:c.2962G>A	XP_024306029.1:p.Ala988Thr
XR_932836.2:n.3107G>A
XR_932837.3:n.3107G>A
XR_932838.3:n.3107G>A
NM_001171.6:c.2926G>A MANE Select	NP_001162.5:p.Ala976Thr