Canonical Allele Identifier: CA2959555

Gene: ALB

Linked Data

• dbSNP Id: rs750844332
• ExAC: 4:74280821 A / C
• gnomAD v2: 4-74280821-A-C
• gnomAD v4: 4-73415104-A-C
• MyVariant Identifiers: chr4:g.74280821A>C (hg19) ; chr4:g.73415104A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415104A>C , CM000666.2:g.73415104A>C	GRCh38
NC_000004.11:g.74280821A>C , CM000666.1:g.74280821A>C	GRCh37
NC_000004.10:g.74499685A>C	NCBI36
NG_009291.1:g.15850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1128A>C MANE Select	ENSP00000295897.4:p.Thr376=
ENST00000295897.8:c.1128A>C	ENSP00000295897.4:p.Thr376=
ENST00000401494.7:c.783A>C	ENSP00000384695.3:p.Thr261=
ENST00000415165.6:c.552A>C	ENSP00000401820.2:p.Thr184=
ENST00000476441.6:c.*407A>C	ENSP00000423727.1:n.*407A>C
ENST00000484992.1:n.448A>C
ENST00000503124.5:c.678A>C	ENSP00000421027.1:p.Thr226=
ENST00000504043.1:n.131A>C
ENST00000505649.5:n.814A>C
ENST00000509063.5:c.1128A>C	ENSP00000422784.1:p.Thr376=
ENST00000511370.1:c.661A>C
ENST00000621085.4:c.491-2A>C	ENSP00000483421.1:n.491-2A>C
ENST00000621628.4:c.489A>C	ENSP00000480485.1:p.Thr163=
NM_000477.5:c.1128A>C	NP_000468.1:p.Thr376=
NM_000477.6:c.1128A>C	NP_000468.1:p.Thr376=
NM_000477.7:c.1128A>C MANE Select	NP_000468.1:p.Thr376=