Canonical Allele Identifier: CA394880442

Gene: ABCC6

Linked Data

• dbSNP Id: rs2046769494
• MyVariant Identifiers: chr16:g.16256878T>A (hg19) ; chr16:g.16163021T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163021T>A , CM000678.2:g.16163021T>A	GRCh38
NC_000016.9:g.16256878T>A , CM000678.1:g.16256878T>A	GRCh37
NC_000016.8:g.16164379T>A	NCBI36
NG_007558.2:g.65451A>T
NG_007558.3:g.65597A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3478A>T	ENSP00000483331.2:p.Ile1160Phe
ENST00000205557.12:c.3478A>T MANE Select	ENSP00000205557.7:p.Ile1160Phe
ENST00000640696.1:c.321-1457A>T	ENSP00000492197.1:n.321-1457A>T
ENST00000205557.11:c.3478A>T	ENSP00000205557.7:p.Ile1160Phe
ENST00000456970.6:c.3132-1457A>T	ENSP00000405002.2:n.3132-1457A>T
ENST00000622290.4:c.*687A>T	ENSP00000483331.1:n.*687A>T
NM_001171.5:c.3478A>T	NP_001162.4:p.Ile1160Phe
XM_011522479.1:c.3445A>T	XP_011520781.1:p.Ile1149Phe
XM_011522480.1:c.3136A>T	XP_011520782.1:p.Ile1046Phe
XM_011522481.1:c.3136A>T	XP_011520783.1:p.Ile1046Phe
XR_932836.1:n.3713A>T
XR_932837.1:n.3543-1457A>T
XR_932838.1:n.3543-1457A>T
XR_933133.1:n.407+178T>A
XR_933134.1:n.754+178T>A
NM_001351800.1:c.3136A>T	NP_001338729.1:p.Ile1046Phe
NR_147784.1:n.3169-1457A>T
XM_011522479.2:c.3445A>T	XP_011520781.1:p.Ile1149Phe
XM_011522481.3:c.3136A>T	XP_011520783.1:p.Ile1046Phe
XM_017023212.1:c.3310A>T	XP_016878701.1:p.Ile1104Phe
XM_017023214.1:c.3307-1457A>T	XP_016878703.1:n.3307-1457A>T
XM_024450261.1:c.3514A>T	XP_024306029.1:p.Ile1172Phe
XR_932836.2:n.3659A>T
XR_932837.3:n.3488-1457A>T
XR_932838.3:n.3488-1457A>T
NM_001171.6:c.3478A>T MANE Select	NP_001162.5:p.Ile1160Phe