Canonical Allele Identifier: CA394878990

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253442T>C (hg19) ; chr16:g.16159585T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159585T>C , CM000678.2:g.16159585T>C	GRCh38
NC_000016.9:g.16253442T>C , CM000678.1:g.16253442T>C	GRCh37
NC_000016.8:g.16160943T>C	NCBI36
NG_007558.2:g.68887A>G
NG_007558.3:g.69033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3634-2A>G	ENSP00000483331.2:n.3634-2A>G
ENST00000205557.12:c.3634-2A>G MANE Select	ENSP00000205557.7:n.3634-2A>G
ENST00000640696.1:c.448-2A>G	ENSP00000492197.1:n.448-2A>G
ENST00000205557.11:c.3634-2A>G	ENSP00000205557.7:n.3634-2A>G
ENST00000456970.6:c.3259-2A>G	ENSP00000405002.2:n.3259-2A>G
ENST00000622290.4:c.*843-2A>G	ENSP00000483331.1:n.*843-2A>G
NM_001171.5:c.3634-2A>G	NP_001162.4:n.3634-2A>G
XM_011522479.1:c.3601-2A>G	XP_011520781.1:n.3601-2A>G
XM_011522480.1:c.3292-2A>G	XP_011520782.1:n.3292-2A>G
XM_011522481.1:c.3292-2A>G	XP_011520783.1:n.3292-2A>G
XR_932836.1:n.3869-2A>G
XR_932837.1:n.3670-2A>G
XR_932838.1:n.3670-2A>G
XR_933134.1:n.539-196T>C
NM_001351800.1:c.3292-2A>G	NP_001338729.1:n.3292-2A>G
NR_147784.1:n.3296-2A>G
XM_011522479.2:c.3601-2A>G	XP_011520781.1:n.3601-2A>G
XM_011522481.3:c.3292-2A>G	XP_011520783.1:n.3292-2A>G
XM_017023212.1:c.3466-2A>G	XP_016878701.1:n.3466-2A>G
XM_024450261.1:c.3670-2A>G	XP_024306029.1:n.3670-2A>G
XR_932836.2:n.3815-2A>G
XR_932837.3:n.3615-2A>G
XR_932838.3:n.3615-2A>G
NM_001171.6:c.3634-2A>G MANE Select	NP_001162.5:n.3634-2A>G