Canonical Allele Identifier: CA99706828

Gene: ALB

Linked Data

• dbSNP Id: rs993768386
• gnomAD v3: 4-73414753-C-T
• gnomAD v4: 4-73414753-C-T
• MyVariant Identifiers: chr4:g.74280470C>T (hg19) ; chr4:g.73414753C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414753C>T , CM000666.2:g.73414753C>T	GRCh38
NC_000004.11:g.74280470C>T , CM000666.1:g.74280470C>T	GRCh37
NC_000004.10:g.74499334C>T	NCBI36
NG_009291.1:g.15499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-282C>T MANE Select	ENSP00000295897.4:n.1059-282C>T
ENST00000295897.8:c.1059-282C>T	ENSP00000295897.4:n.1059-282C>T
ENST00000401494.7:c.714-282C>T	ENSP00000384695.3:n.714-282C>T
ENST00000415165.6:c.483-282C>T	ENSP00000401820.2:n.483-282C>T
ENST00000476441.6:c.*338-282C>T	ENSP00000423727.1:n.*338-282C>T
ENST00000484992.1:n.379-282C>T
ENST00000503124.5:c.609-282C>T	ENSP00000421027.1:n.609-282C>T
ENST00000504043.1:n.62-282C>T
ENST00000505649.5:n.745-282C>T
ENST00000509063.5:c.1059-282C>T	ENSP00000422784.1:n.1059-282C>T
ENST00000511370.1:c.592-282C>T
ENST00000621085.4:c.491-353C>T	ENSP00000483421.1:n.491-353C>T
ENST00000621628.4:c.487-349C>T	ENSP00000480485.1:n.487-349C>T
NM_000477.5:c.1059-282C>T	NP_000468.1:n.1059-282C>T
NM_000477.6:c.1059-282C>T	NP_000468.1:n.1059-282C>T
NM_000477.7:c.1059-282C>T MANE Select	NP_000468.1:n.1059-282C>T