Canonical Allele Identifier: CA2119340

Linked Data

dbSNP Id: rs563880197

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219213844G>A , CM000664.2:g.219213844G>A GRCh38
NC_000002.11:g.220078566G>A , CM000664.1:g.220078566G>A GRCh37
NC_000002.10:g.219786810G>A NCBI36
NG_032110.1:g.10147C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265316.9:c.1560C>T (ABCB6) MANE Select ENSP00000265316.3:p.Val520=
ENST00000295750.5:c.1422C>T (ABCB6) ENSP00000295750.5:p.Val474=
ENST00000265316.7:c.1560C>T (ABCB6) ENSP00000265316.3:p.Val520=
ENST00000295750.4:c.1103C>T (ABCB6)
ENST00000446716.5:c.4285C>T (ATG9A)
ENST00000448398.5:c.636C>T (ABCB6)
ENST00000494639.5:n.469C>T (ABCB6)
ENST00000497882.5:n.1873C>T (ABCB6)
NM_005689.2:c.1560C>T (ABCB6) NP_005680.1:p.Val520=
NM_001349828.1:c.1422C>T (ABCB6) NP_001336757.1:p.Val474=
NM_005689.3:c.1560C>T (ABCB6) NP_005680.1:p.Val520=
NM_005689.4:c.1560C>T (ABCB6) MANE Select NP_005680.1:p.Val520=
NM_001349828.2:c.1422C>T (ABCB6) NP_001336757.1:p.Val474=