Canonical Allele Identifier: CA2600249919

Gene: ALB

Linked Data

• dbSNP Id: rs2149328789
• gnomAD v3: 4-73414987-T-C
• gnomAD v4: 4-73414987-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414987T>C , CM000666.2:g.73414987T>C	GRCh38
NC_000004.11:g.74280704T>C , CM000666.1:g.74280704T>C	GRCh37
NC_000004.10:g.74499568T>C	NCBI36
NG_009291.1:g.15733T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059-48T>C MANE Select	ENSP00000295897.4:n.1059-48T>C
ENST00000295897.8:c.1059-48T>C	ENSP00000295897.4:n.1059-48T>C
ENST00000401494.7:c.714-48T>C	ENSP00000384695.3:n.714-48T>C
ENST00000415165.6:c.483-48T>C	ENSP00000401820.2:n.483-48T>C
ENST00000476441.6:c.*338-48T>C	ENSP00000423727.1:n.*338-48T>C
ENST00000484992.1:n.379-48T>C
ENST00000503124.5:c.609-48T>C	ENSP00000421027.1:n.609-48T>C
ENST00000504043.1:n.62-48T>C
ENST00000505649.5:n.745-48T>C
ENST00000509063.5:c.1059-48T>C	ENSP00000422784.1:n.1059-48T>C
ENST00000511370.1:c.592-48T>C
ENST00000621085.4:c.491-119T>C	ENSP00000483421.1:n.491-119T>C
ENST00000621628.4:c.487-115T>C	ENSP00000480485.1:n.487-115T>C
NM_000477.5:c.1059-48T>C	NP_000468.1:n.1059-48T>C
NM_000477.6:c.1059-48T>C	NP_000468.1:n.1059-48T>C
NM_000477.7:c.1059-48T>C MANE Select	NP_000468.1:n.1059-48T>C