Canonical Allele Identifier: CA1787831710

Gene: CA8

Linked Data

• dbSNP Id: rs1806162928

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192657G>C , CM000670.2:g.60192657G>C	GRCh38
NC_000008.10:g.61105216G>C , CM000670.1:g.61105216G>C	GRCh37
NC_000008.9:g.61267770G>C	NCBI36
NG_023193.1:g.93739C>G
NG_023193.2:g.93739C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317995.5:c.*36-2672C>G MANE Select	ENSP00000314407.4:n.*36-2672C>G
ENST00000317995.4:c.*36-2672C>G	ENSP00000314407.4:n.*36-2672C>G
NM_004056.4:c.*36-2672C>G	NP_004047.3:n.*36-2672C>G
XM_011517586.1:c.*36-2672C>G	XP_011515888.1:n.*36-2672C>G
NM_001321839.1:c.*36-2672C>G	NP_001308768.1:n.*36-2672C>G
NM_004056.5:c.*36-2672C>G	NP_004047.3:n.*36-2672C>G
NR_135821.1:n.1235-2672C>G
XM_017013818.1:c.*36-2672C>G	XP_016869307.1:n.*36-2672C>G
NM_004056.6:c.*36-2672C>G MANE Select	NP_004047.3:n.*36-2672C>G
NM_001321839.2:c.*36-2672C>G	NP_001308768.1:n.*36-2672C>G
NR_135821.2:n.1212-2672C>G