Canonical Allele Identifier: CA99707040
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs990726722

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73414978T>C , CM000666.2:g.73414978T>C GRCh38
NC_000004.11:g.74280695T>C , CM000666.1:g.74280695T>C GRCh37
NC_000004.10:g.74499559T>C NCBI36
NG_009291.1:g.15724T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-57T>C MANE Select ENSP00000295897.4:n.1059-57T>C
ENST00000295897.8:c.1059-57T>C ENSP00000295897.4:n.1059-57T>C
ENST00000401494.7:c.714-57T>C ENSP00000384695.3:n.714-57T>C
ENST00000415165.6:c.483-57T>C ENSP00000401820.2:n.483-57T>C
ENST00000476441.6:c.*338-57T>C ENSP00000423727.1:n.*338-57T>C
ENST00000484992.1:n.379-57T>C
ENST00000503124.5:c.609-57T>C ENSP00000421027.1:n.609-57T>C
ENST00000504043.1:n.62-57T>C
ENST00000505649.5:n.745-57T>C
ENST00000509063.5:c.1059-57T>C ENSP00000422784.1:n.1059-57T>C
ENST00000511370.1:c.592-57T>C
ENST00000621085.4:c.491-128T>C ENSP00000483421.1:n.491-128T>C
ENST00000621628.4:c.487-124T>C ENSP00000480485.1:n.487-124T>C
NM_000477.5:c.1059-57T>C NP_000468.1:n.1059-57T>C
NM_000477.6:c.1059-57T>C NP_000468.1:n.1059-57T>C
NM_000477.7:c.1059-57T>C MANE Select NP_000468.1:n.1059-57T>C