Canonical Allele Identifier: CA394880540

Gene: ABCC6

Linked Data

• dbSNP Id: rs2046770412
• gnomAD v3: 16-16163036-C-A
• gnomAD v4: 16-16163036-C-A
• MyVariant Identifiers: chr16:g.16256893C>A (hg19) ; chr16:g.16163036C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163036C>A , CM000678.2:g.16163036C>A	GRCh38
NC_000016.9:g.16256893C>A , CM000678.1:g.16256893C>A	GRCh37
NC_000016.8:g.16164394C>A	NCBI36
NG_007558.2:g.65436G>T
NG_007558.3:g.65582G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3463G>T	ENSP00000483331.2:p.Asp1155Tyr
ENST00000205557.12:c.3463G>T MANE Select	ENSP00000205557.7:p.Asp1155Tyr
ENST00000640696.1:c.321-1472G>T	ENSP00000492197.1:n.321-1472G>T
ENST00000205557.11:c.3463G>T	ENSP00000205557.7:p.Asp1155Tyr
ENST00000456970.6:c.3132-1472G>T	ENSP00000405002.2:n.3132-1472G>T
ENST00000622290.4:c.*672G>T	ENSP00000483331.1:n.*672G>T
NM_001171.5:c.3463G>T	NP_001162.4:p.Asp1155Tyr
XM_011522479.1:c.3430G>T	XP_011520781.1:p.Asp1144Tyr
XM_011522480.1:c.3121G>T	XP_011520782.1:p.Asp1041Tyr
XM_011522481.1:c.3121G>T	XP_011520783.1:p.Asp1041Tyr
XR_932836.1:n.3698G>T
XR_932837.1:n.3543-1472G>T
XR_932838.1:n.3543-1472G>T
XR_933133.1:n.407+193C>A
XR_933134.1:n.754+193C>A
NM_001351800.1:c.3121G>T	NP_001338729.1:p.Asp1041Tyr
NR_147784.1:n.3169-1472G>T
XM_011522479.2:c.3430G>T	XP_011520781.1:p.Asp1144Tyr
XM_011522481.3:c.3121G>T	XP_011520783.1:p.Asp1041Tyr
XM_017023212.1:c.3295G>T	XP_016878701.1:p.Asp1099Tyr
XM_017023214.1:c.3307-1472G>T	XP_016878703.1:n.3307-1472G>T
XM_024450261.1:c.3499G>T	XP_024306029.1:p.Asp1167Tyr
XR_932836.2:n.3644G>T
XR_932837.3:n.3488-1472G>T
XR_932838.3:n.3488-1472G>T
NM_001171.6:c.3463G>T MANE Select	NP_001162.5:p.Asp1155Tyr