Canonical Allele Identifier: CA394883495

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244022A>G (hg19) ; chr16:g.16150165A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150165A>G , CM000678.2:g.16150165A>G	GRCh38
NC_000016.9:g.16244022A>G , CM000678.1:g.16244022A>G	GRCh37
NC_000016.8:g.16151523A>G	NCBI36
NG_007558.2:g.78307T>C
NG_007558.3:g.78453T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*652T>C	ENSP00000483331.2:n.*652T>C
ENST00000205557.12:c.4480T>C MANE Select	ENSP00000205557.7:p.Tyr1494His
ENST00000640696.1:c.1294T>C	ENSP00000492197.1:p.Tyr432His
ENST00000205557.11:c.4480T>C	ENSP00000205557.7:p.Tyr1494His
ENST00000456970.6:c.4105T>C	ENSP00000405002.2:n.4105T>C
ENST00000576204.5:n.1343T>C
ENST00000622290.4:c.*1689T>C	ENSP00000483331.1:n.*1689T>C
NM_001171.5:c.4480T>C	NP_001162.4:p.Tyr1494His
XM_011522479.1:c.4447T>C	XP_011520781.1:p.Tyr1483His
XM_011522480.1:c.4138T>C	XP_011520782.1:p.Tyr1380His
XM_011522481.1:c.4138T>C	XP_011520783.1:p.Tyr1380His
XR_933134.1:n.538+5875A>G
NM_001351800.1:c.4138T>C	NP_001338729.1:p.Tyr1380His
NR_147784.1:n.4142T>C
XM_011522479.2:c.4447T>C	XP_011520781.1:p.Tyr1483His
XM_011522481.3:c.4138T>C	XP_011520783.1:p.Tyr1380His
XM_017023212.1:c.4312T>C	XP_016878701.1:p.Tyr1438His
XM_024450261.1:c.4516T>C	XP_024306029.1:p.Tyr1506His
NM_001171.6:c.4480T>C MANE Select	NP_001162.5:p.Tyr1494His