Canonical Allele Identifier: CA394884110

Gene: ABCC6

Linked Data

• dbSNP Id: rs1326045319
• gnomAD v3: 16-16150773-C-T
• gnomAD v4: 16-16150773-C-T
• MyVariant Identifiers: chr16:g.16244630C>T (hg19) ; chr16:g.16150773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150773C>T , CM000678.2:g.16150773C>T	GRCh38
NC_000016.9:g.16244630C>T , CM000678.1:g.16244630C>T	GRCh37
NC_000016.8:g.16152131C>T	NCBI36
NG_007558.2:g.77699G>A
NG_007558.3:g.77845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-1G>A	ENSP00000483331.2:n.*381-1G>A
ENST00000205557.12:c.4209-1G>A MANE Select	ENSP00000205557.7:n.4209-1G>A
ENST00000640696.1:c.1023-1G>A	ENSP00000492197.1:n.1023-1G>A
ENST00000205557.11:c.4209-1G>A	ENSP00000205557.7:n.4209-1G>A
ENST00000456970.6:c.3834-1G>A	ENSP00000405002.2:n.3834-1G>A
ENST00000576204.5:n.1072-1G>A
ENST00000622290.4:c.*1418-1G>A	ENSP00000483331.1:n.*1418-1G>A
NM_001171.5:c.4209-1G>A	NP_001162.4:n.4209-1G>A
XM_011522479.1:c.4176-1G>A	XP_011520781.1:n.4176-1G>A
XM_011522480.1:c.3867-1G>A	XP_011520782.1:n.3867-1G>A
XM_011522481.1:c.3867-1G>A	XP_011520783.1:n.3867-1G>A
XR_933134.1:n.538+6483C>T
NM_001351800.1:c.3867-1G>A	NP_001338729.1:n.3867-1G>A
NR_147784.1:n.3871-1G>A
XM_011522479.2:c.4176-1G>A	XP_011520781.1:n.4176-1G>A
XM_011522481.3:c.3867-1G>A	XP_011520783.1:n.3867-1G>A
XM_017023212.1:c.4041-1G>A	XP_016878701.1:n.4041-1G>A
XM_024450261.1:c.4245-1G>A	XP_024306029.1:n.4245-1G>A
NM_001171.6:c.4209-1G>A MANE Select	NP_001162.5:n.4209-1G>A