Canonical Allele Identifier: CA394884405

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263558C>A (hg19) ; chr16:g.16169701C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169701C>A , CM000678.2:g.16169701C>A	GRCh38
NC_000016.9:g.16263558C>A , CM000678.1:g.16263558C>A	GRCh37
NC_000016.8:g.16171059C>A	NCBI36
NG_007558.2:g.58771G>T
NG_007558.3:g.58917G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2940G>T	ENSP00000483331.2:p.Gln980His
ENST00000205557.12:c.2940G>T MANE Select	ENSP00000205557.7:p.Gln980His
ENST00000205557.11:c.2940G>T	ENSP00000205557.7:p.Gln980His
ENST00000456970.6:c.2765G>T	ENSP00000405002.2:n.2765G>T
ENST00000622290.4:c.*149G>T	ENSP00000483331.1:n.*149G>T
NM_001171.5:c.2940G>T	NP_001162.4:p.Gln980His
XM_011522479.1:c.2907G>T	XP_011520781.1:p.Gln969His
XM_011522480.1:c.2598G>T	XP_011520782.1:p.Gln866His
XM_011522481.1:c.2598G>T	XP_011520783.1:p.Gln866His
XR_932836.1:n.3175G>T
XR_932837.1:n.3176G>T
XR_932838.1:n.3176G>T
NM_001351800.1:c.2598G>T	NP_001338729.1:p.Gln866His
NR_147784.1:n.2802G>T
XM_011522479.2:c.2907G>T	XP_011520781.1:p.Gln969His
XM_011522481.3:c.2598G>T	XP_011520783.1:p.Gln866His
XM_017023212.1:c.2772G>T	XP_016878701.1:p.Gln924His
XM_017023214.1:c.2940G>T	XP_016878703.1:p.Gln980His
XM_024450261.1:c.2976G>T	XP_024306029.1:p.Gln992His
XR_932836.2:n.3121G>T
XR_932837.3:n.3121G>T
XR_932838.3:n.3121G>T
NM_001171.6:c.2940G>T MANE Select	NP_001162.5:p.Gln980His