Canonical Allele Identifier: CA493799606

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263699T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169842T>G , CM000678.2:g.16169842T>G	GRCh38
NC_000016.9:g.16263699T>G , CM000678.1:g.16263699T>G	GRCh37
NC_000016.8:g.16171200T>G	NCBI36
NG_007558.2:g.58630A>C
NG_007558.3:g.58776A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2799A>C	ENSP00000483331.2:p.Thr933=
ENST00000205557.12:c.2799A>C MANE Select	ENSP00000205557.7:p.Thr933=
ENST00000205557.11:c.2799A>C	ENSP00000205557.7:p.Thr933=
ENST00000456970.6:c.2624A>C	ENSP00000405002.2:n.2624A>C
ENST00000622290.4:c.*8A>C	ENSP00000483331.1:n.*8A>C
NM_001171.5:c.2799A>C	NP_001162.4:p.Thr933=
XM_011522479.1:c.2766A>C	XP_011520781.1:p.Thr922=
XM_011522480.1:c.2457A>C	XP_011520782.1:p.Thr819=
XM_011522481.1:c.2457A>C	XP_011520783.1:p.Thr819=
XR_932836.1:n.3034A>C
XR_932837.1:n.3035A>C
XR_932838.1:n.3035A>C
NM_001351800.1:c.2457A>C	NP_001338729.1:p.Thr819=
NR_147784.1:n.2661A>C
XM_011522479.2:c.2766A>C	XP_011520781.1:p.Thr922=
XM_011522481.3:c.2457A>C	XP_011520783.1:p.Thr819=
XM_017023212.1:c.2631A>C	XP_016878701.1:p.Thr877=
XM_017023214.1:c.2799A>C	XP_016878703.1:p.Thr933=
XM_024450261.1:c.2835A>C	XP_024306029.1:p.Thr945=
XR_932836.2:n.2980A>C
XR_932837.3:n.2980A>C
XR_932838.3:n.2980A>C
NM_001171.6:c.2799A>C MANE Select	NP_001162.5:p.Thr933=