Canonical Allele Identifier: CA7925342

Gene: ABCC6

Linked Data

• dbSNP Id: rs767444769
• ExAC: 16:16248704 T / A
• gnomAD v2: 16-16248704-T-A
• gnomAD v4: 16-16154847-T-A
• MyVariant Identifiers: chr16:g.16248704T>A (hg19) ; chr16:g.16154847T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154847T>A , CM000678.2:g.16154847T>A	GRCh38
NC_000016.9:g.16248704T>A , CM000678.1:g.16248704T>A	GRCh37
NC_000016.8:g.16156205T>A	NCBI36
NG_007558.2:g.73625A>T
NG_007558.3:g.73771A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.904+26A>T
ENST00000622290.5:c.*213+26A>T	ENSP00000483331.2:n.*213+26A>T
ENST00000205557.12:c.4041+26A>T MANE Select	ENSP00000205557.7:n.4041+26A>T
ENST00000640696.1:c.855+26A>T	ENSP00000492197.1:n.855+26A>T
ENST00000205557.11:c.4041+26A>T	ENSP00000205557.7:n.4041+26A>T
ENST00000456970.6:c.3666+26A>T	ENSP00000405002.2:n.3666+26A>T
ENST00000576204.5:n.904+26A>T
ENST00000622290.4:c.*1250+26A>T	ENSP00000483331.1:n.*1250+26A>T
NM_001171.5:c.4041+26A>T	NP_001162.4:n.4041+26A>T
XM_011522479.1:c.4008+26A>T	XP_011520781.1:n.4008+26A>T
XM_011522480.1:c.3699+26A>T	XP_011520782.1:n.3699+26A>T
XM_011522481.1:c.3699+26A>T	XP_011520783.1:n.3699+26A>T
XR_933134.1:n.539-4934T>A
NM_001351800.1:c.3699+26A>T	NP_001338729.1:n.3699+26A>T
NR_147784.1:n.3703+26A>T
XM_011522479.2:c.4008+26A>T	XP_011520781.1:n.4008+26A>T
XM_011522481.3:c.3699+26A>T	XP_011520783.1:n.3699+26A>T
XM_017023212.1:c.3873+26A>T	XP_016878701.1:n.3873+26A>T
XM_024450261.1:c.4077+26A>T	XP_024306029.1:n.4077+26A>T
NM_001171.6:c.4041+26A>T MANE Select	NP_001162.5:n.4041+26A>T