Canonical Allele Identifier: CA278636155

Gene: ABCC6

Linked Data

• ClinVar Variation Id: 1985895
• ClinVar RCV Id: RCV002785777
• dbSNP Id: rs913530470
• gnomAD v3: 16-16169733-G-A
• gnomAD v4: 16-16169733-G-A
• MyVariant Identifiers: chr16:g.16263590G>A (hg19) ; chr16:g.16169733G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169733G>A , CM000678.2:g.16169733G>A	GRCh38
NC_000016.9:g.16263590G>A , CM000678.1:g.16263590G>A	GRCh37
NC_000016.8:g.16171091G>A	NCBI36
NG_007558.2:g.58739C>T
NG_007558.3:g.58885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2908C>T	ENSP00000483331.2:p.Leu970=
ENST00000205557.12:c.2908C>T MANE Select	ENSP00000205557.7:p.Leu970=
ENST00000205557.11:c.2908C>T	ENSP00000205557.7:p.Leu970=
ENST00000456970.6:c.2733C>T	ENSP00000405002.2:n.2733C>T
ENST00000622290.4:c.*117C>T	ENSP00000483331.1:n.*117C>T
NM_001171.5:c.2908C>T	NP_001162.4:p.Leu970=
XM_011522479.1:c.2875C>T	XP_011520781.1:p.Leu959=
XM_011522480.1:c.2566C>T	XP_011520782.1:p.Leu856=
XM_011522481.1:c.2566C>T	XP_011520783.1:p.Leu856=
XR_932836.1:n.3143C>T
XR_932837.1:n.3144C>T
XR_932838.1:n.3144C>T
NM_001351800.1:c.2566C>T	NP_001338729.1:p.Leu856=
NR_147784.1:n.2770C>T
XM_011522479.2:c.2875C>T	XP_011520781.1:p.Leu959=
XM_011522481.3:c.2566C>T	XP_011520783.1:p.Leu856=
XM_017023212.1:c.2740C>T	XP_016878701.1:p.Leu914=
XM_017023214.1:c.2908C>T	XP_016878703.1:p.Leu970=
XM_024450261.1:c.2944C>T	XP_024306029.1:p.Leu982=
XR_932836.2:n.3089C>T
XR_932837.3:n.3089C>T
XR_932838.3:n.3089C>T
NM_001171.6:c.2908C>T MANE Select	NP_001162.5:p.Leu970=