Canonical Allele Identifier: CA1787861889

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60281419G= , CM000670.2:g.60281419G=	GRCh38
NC_000008.10:g.61193978G= , CM000670.1:g.61193978G=	GRCh37
NC_000008.9:g.61356532G=	NCBI36
NG_023193.1:g.4977C=
NG_023193.2:g.4977C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001321837.1:c.-272C=	NP_001308766.1:n.-272C=
NM_001321838.1:c.-272C=	NP_001308767.1:n.-272C=
NM_001321839.1:c.-272C=	NP_001308768.1:n.-272C=
NM_004056.5:c.-272C=	NP_004047.3:n.-272C=
NR_135821.1:n.5C=