Canonical Allele Identifier: CA99712629
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs75738598
MyVariant Identifiers: chr4:g.74285979A>C (hg19) chr4:g.73420262A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420262A>C , CM000666.2:g.73420262A>C GRCh38
NC_000004.11:g.74285979A>C , CM000666.1:g.74285979A>C GRCh37
NC_000004.10:g.74504843A>C NCBI36
NG_009291.1:g.21008A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1794A>C MANE Select ENSP00000295897.4:p.Lys598Asn
ENST00000295897.8:c.1794A>C ENSP00000295897.4:p.Lys598Asn
ENST00000401494.7:c.1449A>C ENSP00000384695.3:p.Lys483Asn
ENST00000415165.6:c.1218A>C ENSP00000401820.2:p.Lys406Asn
ENST00000476441.6:c.*1073A>C ENSP00000423727.1:n.*1073A>C
ENST00000495173.1:n.102A>C
ENST00000503124.5:c.1344A>C ENSP00000421027.1:p.Lys448Asn
ENST00000505649.5:n.1341A>C
ENST00000508932.5:n.184A>C
ENST00000509063.5:c.1785+623A>C ENSP00000422784.1:n.1785+623A>C
ENST00000511370.1:c.1327A>C
ENST00000621085.4:c.1155A>C ENSP00000483421.1:p.Lys385Asn
ENST00000621628.4:c.1155A>C ENSP00000480485.1:p.Lys385Asn
NM_000477.5:c.1794A>C NP_000468.1:p.Lys598Asn
NM_000477.6:c.1794A>C NP_000468.1:p.Lys598Asn
NM_000477.7:c.1794A>C MANE Select NP_000468.1:p.Lys598Asn
Search 100 bp 5'
Search 100 bp 3'