Canonical Allele Identifier: CA493798908

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16256858C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163001C>G , CM000678.2:g.16163001C>G	GRCh38
NC_000016.9:g.16256858C>G , CM000678.1:g.16256858C>G	GRCh37
NC_000016.8:g.16164359C>G	NCBI36
NG_007558.2:g.65471G>C
NG_007558.3:g.65617G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3498G>C	ENSP00000483331.2:p.Val1166=
ENST00000205557.12:c.3498G>C MANE Select	ENSP00000205557.7:p.Val1166=
ENST00000640696.1:c.321-1437G>C	ENSP00000492197.1:n.321-1437G>C
ENST00000205557.11:c.3498G>C	ENSP00000205557.7:p.Val1166=
ENST00000456970.6:c.3132-1437G>C	ENSP00000405002.2:n.3132-1437G>C
ENST00000622290.4:c.*707G>C	ENSP00000483331.1:n.*707G>C
NM_001171.5:c.3498G>C	NP_001162.4:p.Val1166=
XM_011522479.1:c.3465G>C	XP_011520781.1:p.Val1155=
XM_011522480.1:c.3156G>C	XP_011520782.1:p.Val1052=
XM_011522481.1:c.3156G>C	XP_011520783.1:p.Val1052=
XR_932836.1:n.3733G>C
XR_932837.1:n.3543-1437G>C
XR_932838.1:n.3543-1437G>C
XR_933133.1:n.407+158C>G
XR_933134.1:n.754+158C>G
NM_001351800.1:c.3156G>C	NP_001338729.1:p.Val1052=
NR_147784.1:n.3169-1437G>C
XM_011522479.2:c.3465G>C	XP_011520781.1:p.Val1155=
XM_011522481.3:c.3156G>C	XP_011520783.1:p.Val1052=
XM_017023212.1:c.3330G>C	XP_016878701.1:p.Val1110=
XM_017023214.1:c.3307-1437G>C	XP_016878703.1:n.3307-1437G>C
XM_024450261.1:c.3534G>C	XP_024306029.1:p.Val1178=
XR_932836.2:n.3679G>C
XR_932837.3:n.3488-1437G>C
XR_932838.3:n.3488-1437G>C
NM_001171.6:c.3498G>C MANE Select	NP_001162.5:p.Val1166=