Canonical Allele Identifier: CA439800256

Gene: ALB

Linked Data

• dbSNP Id: rs1157631720
• gnomAD v2: 4-74280761-T-C
• gnomAD v4: 4-73415044-T-C
• MyVariant Identifiers: chr4:g.74280761T>C (hg19) ; chr4:g.73415044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415044T>C , CM000666.2:g.73415044T>C	GRCh38
NC_000004.11:g.74280761T>C , CM000666.1:g.74280761T>C	GRCh37
NC_000004.10:g.74499625T>C	NCBI36
NG_009291.1:g.15790T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1068T>C MANE Select	ENSP00000295897.4:p.Tyr356=
ENST00000295897.8:c.1068T>C	ENSP00000295897.4:p.Tyr356=
ENST00000401494.7:c.723T>C	ENSP00000384695.3:p.Tyr241=
ENST00000415165.6:c.492T>C	ENSP00000401820.2:p.Tyr164=
ENST00000476441.6:c.*347T>C	ENSP00000423727.1:n.*347T>C
ENST00000484992.1:n.388T>C
ENST00000503124.5:c.618T>C	ENSP00000421027.1:p.Tyr206=
ENST00000504043.1:n.71T>C
ENST00000505649.5:n.754T>C
ENST00000509063.5:c.1068T>C	ENSP00000422784.1:p.Tyr356=
ENST00000511370.1:c.601T>C
ENST00000621085.4:c.491-62T>C	ENSP00000483421.1:n.491-62T>C
ENST00000621628.4:c.487-58T>C	ENSP00000480485.1:n.487-58T>C
NM_000477.5:c.1068T>C	NP_000468.1:p.Tyr356=
NM_000477.6:c.1068T>C	NP_000468.1:p.Tyr356=
NM_000477.7:c.1068T>C MANE Select	NP_000468.1:p.Tyr356=