Canonical Allele Identifier: CA1468143161

Gene: ALB

Linked Data

• dbSNP Id: rs1718971655

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414747G>C , CM000666.2:g.73414747G>C	GRCh38
NC_000004.11:g.74280464G>C , CM000666.1:g.74280464G>C	GRCh37
NC_000004.10:g.74499328G>C	NCBI36
NG_009291.1:g.15493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-288G>C MANE Select	ENSP00000295897.4:n.1059-288G>C
ENST00000295897.8:c.1059-288G>C	ENSP00000295897.4:n.1059-288G>C
ENST00000401494.7:c.714-288G>C	ENSP00000384695.3:n.714-288G>C
ENST00000415165.6:c.483-288G>C	ENSP00000401820.2:n.483-288G>C
ENST00000476441.6:c.*338-288G>C	ENSP00000423727.1:n.*338-288G>C
ENST00000484992.1:n.379-288G>C
ENST00000503124.5:c.609-288G>C	ENSP00000421027.1:n.609-288G>C
ENST00000504043.1:n.62-288G>C
ENST00000505649.5:n.745-288G>C
ENST00000509063.5:c.1059-288G>C	ENSP00000422784.1:n.1059-288G>C
ENST00000511370.1:c.592-288G>C
ENST00000621085.4:c.491-359G>C	ENSP00000483421.1:n.491-359G>C
ENST00000621628.4:c.487-355G>C	ENSP00000480485.1:n.487-355G>C
NM_000477.5:c.1059-288G>C	NP_000468.1:n.1059-288G>C
NM_000477.6:c.1059-288G>C	NP_000468.1:n.1059-288G>C
NM_000477.7:c.1059-288G>C MANE Select	NP_000468.1:n.1059-288G>C